|
Doenças Autossômicas Recessivas, Painel para Compatibilidade Genética para Casais |
Painel por Sequenciamento de Próxima Geração + Análise de Deleção/Duplicação |
ABCB11, ABCC8, ABCD1, ACAD9, ACADM, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADGRG1, AGA, AGL, AGPS, AGXT, AIRE, ALDH3A2, ALDOB, ALG6, ALMS1, ALPL, AMT, AQP2, ARG1, ARSA, ARSB, ASL, ASNS, ASPA, ASS1, ATM, ATP6V1B1, ATP7A, ATP7B, ATRX, BBS1, BBS10, BBS12, BBS2, BCKDHA, BCKDHB, BCS1L, BLM, BSND, CAPN3, CBS, CDH23, CEP290, CERKL, CFTR, CHM, CHRNE, CIITA, CLN3, CLN5, CLN6, CLN8, CLRN1, CNGB3, COL27A1, COL4A3, COL4A4, COL4A5, COL7A1, CPS1, CPT1A, CPT2, CRB1, CTNS, CTSK, CYBA, CYBB, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP27A1, DBT, DCLRE1C, DHCR7, DHDDS, DLD, DMD, DNAH5, DNAI1, DNAI2, DYSF, EDA, EIF2B5, ELP1, EMD, ERCC6, ERCC8, ESCO2, ETFA, ETFDH, ETHE1, EVC, EVC2, EYS, F9, FAH, FAM161A, FANCA, FANCC, FANCG, FH, FKRP, FKTN, FMR1, G6PC, GAA, GALC, GALK1, GALT, GAMT, GBA, GBE1, GCDH, GFM1, GJB1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPTAB, GNPTG, GNS, GRHPR, HADHA, HAX1, HBA1, HBA2, HBB, HEXA, HEXB, HGSNAT, HJV, HLCS, HMGCL, HOGA1, HPS1, HPS3, HSD17B4, HSD3B2, HYAL1, HYLS1, IDS, IDUA, IL2RG, IVD, KCNJ11, LAMA2, LAMA3 |
|
Câncer Hereditário |
Painel por Sequenciamento de Próxima Geração |
ACD, AIP, AKT1, ALK, ANKRD26, APC, ARMC5, ASCL1, ASXL1, ATM, ATR, AXIN2, BAP1, BARD1, BDNF, BLM, BMPR1A, BRAF, BRCA1, BRCA2, BRIP1, BUB1B, CASP10, CASP9, CBL, CDC73, CDH1, CDH23, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, CEP57, CHEK2, CREBBP, CSF3R, CTC1, CTNNA1, CTNNB1, CYLD, DDB2, DDX41, DICER1, DIS3L2, DKC1, DNAJC21, DNMT3B, DOCK8, EDN3, EGFR, EPCAM, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC6L2, ETV6, EXT1, EXT2, EZH2, FAN1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAS, FASLG, FH, FLCN, G6PC, GATA1, GATA2, GDNF, GLMN, GNAS, GPC3, GREM1, H19, HCLS1, HNF1A, HOXB13, HRAS, IPMK, JAG1, JAK2, KIF1B, KIT, KLLN, KRAS, LAPTM5, LIG4, LZTR1, MAD2L2, MAGT1, MAP2K1, MAP2K2, MAP3K1, MAX, MEN1, MET, MITF, MLH1, MLH3, MMP1, MNX1, MRE11, MSH2, MSH3, MSH6, MSR1, MTAP, MUTYH, NBN, NF1, NF2, NHP2, NME1, NOP10, NRAS, NSD1, NTHL1, NTRK1, PALB2, PARN, PAX5, PBRM1, PDGFB, PDGFRA, PDGFRB, PHOX2B, PIK3CA, PMS2, POLD1, POLE, POLH, POT1, PRF1, PRKAR1A, PSMC3IP, PTCH1, PTCH2, PTEN, PTPN11, RAD50, RAD51, RAD51C |
|
Câncer de Prostata, Painel Expandido |
Painel por Sequenciamento de Próxima Geração |
AR, ATM, BRCA1, BRCA2, BRIP1, CHEK2, EHBP1, ELAC2, EPCAM, EPHB2, FANCA, HOXB13, MLH1, MSH2, MSH6, MSMB, MSMP, NBN, PALB2, PBOV1, SLC45A3, PMS2, RAD51C, RAD51D, RNASEL, TP53 |
|
Ataxias |
Painel por Sequenciamento de Próxima Geração |
ABHD12, ACO2, AFG3L2, ANO10, APOB, APTX, ATCAY, ATM, ATP8A2, BEAN1, CACNA1A, CACNA1G, CACNB4, CCDC88C, CLCN2, CLN5, COQ2, COQ8A, CYP27A1, DNMT1, ELOVL4, FGF14, FLVCR1, FXN, GOSR2, GRM1, ITPR1, KCNA1, KCNC3, KCND3, KCNJ10, LAMA1, MRE11, MTTP, NOP56, NPC1, NPC2, PDSS1, PDSS2, PDYN, PEX7, PHYH, PMPCA, PNKP, PNPLA6, POLG, PRKCG, PTF1A, RUBCN, SACS, SCN2A, SETX, SIL1, SLC1A3, SPG7, SPTBN2, SYNE1, SYT14, TDP1, TGM6, TPP1, TTBK2, TTPA, TWNK, TXN2, VLDLR, WDR73, WFS1, WWOX |
|
Imunodeficiência e Doenças Imunológicas |
Painel por Sequenciamento de Próxima Geração |
A2ML1 ABCD4, ACD ACP5, ADA, ADAM17, ADNP, AGA, AICDA, AIRE, AK2, ALG1, ALG12, AP3B1, ARMC4 ARPC1B, ATM, B2M, BCL10, BCL11B, BLM, BLNK, BRCA1, BRCA2, BRIP1, BTK, BUB1B, C11orf70, C1QA, C1QB C1QC, C1R, C1S, C2, C21orf59, C3, C5, C6, C7, C8A, C8B, C8ORF37, CARD11, CARD9, CASP10, CASP8, CCBE1 CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CD19, CD247, CD27, CD3D, CD3E, CD3G CD40, CD40LG, CD55, CD59, CD79A, CD79B, CD81, CD8A, CDCA7, CDSN, CEBPE, CECR1, CFB, CFD, CFH, CFI CFP, CHAMP1, CHD1, CHD7, CIITA, CLEC7A, CLPB, COG6, COG7, CORO1A, CPN1, CR2, CREBBP, CRIPT, CSF3R CTC1, CTLA4, CTPS1, CXCR4, CYBA, CYBB, DCLRE1C, DEAF1, DHFR, DKC1, DNAAF1, DNAAF2, DNAAF3, DNAAF5 DNAH1, DNAH11, DNAH5, DNAI1, DNAI2, DNAJC21, DNAL1, DNASE1L3, DNMT3B, DOCK2, DOCK8, DRC1, DSG1 DYX1C1, EFL1, EGFR, ELANE, EPG5, ERCC2, ERCC4, ERCC6L2, ETV6, EXTL3, F12, FADD, FANCA, FANCB FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAZ, FASLG, FAT4, FBXL4, FCGR2C, FCGR3A FCN3, FERMT3, FMO3, FOXN1, FOXP3, G6PC3, GALNS, GAS8, GATA1, G |
|
Câncer Hereditário |
Painel por Sequenciamento de Próxima Geração |
APC, ATM, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, GREM1, MEN1, MET, MLH1, MRE11A, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PALLD, PMS2, POLD1, POLE, PTCH1, PTEN, RAD50, RAD51C, RECQL, RET, SMAD4, STK11, TP53, VHL |
|
Ataxia Espinocerebelar |
Painel por Sequenciamento de Próxima Geração |
SLC52A2, COG5, SLC25A46, KCNC1, FAT2, PLD3, SCYL1, UBA5, KIF26B, EP300, FAT1, XRCC1, VPS13D, FA2H, AAAS, ABCB7, ABHD5, ABHD12, ACADVL, ACO2, ADCK3, AFG3L2, AMPD2, ANO10, AP1S2, APOB, APTX, ARSA, ATCAY, ATM, ATN1, ATP1A3, ATP8A2, ATP2B3, C10ORF2, CA8, CACNA1G, CACNB4, CAMTA1, CASK, CCDC88C, CHMP1A, CLCN2, CLN5, CLN6, COQ2, COX20, CP, CWF19L1, CYP27A1, CYP2U1, DARS2, DDHD2, DNAJC5, DNMT1, DRD3, EEF2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELOVL4, ELOVL5, EPM2A, EXOSC3, FGF14, FLVCR1, FMR1, FOLR1, FUS, FXN, GBA2, GFAP, GJC2, GOS, GOSR2, GRID2, GRM1, HEXA, HEXB, IFRD1, ITPR1, KCNA1, KCNC3, KCND3, KCNJ10, KIF1C, LAMA1, MARS2, MMACHC, MRE11A, MTPAP, MTTP, NHLRC1, NPC1, NPC2, OPHN1, PAX6, PDSS1, PDSS2, PDYN, PEX7, PEX16, PHYH, PLA2G6, PMPCA, PNKP, PNPLA6, POLG, POLR3A, PRKCG, PRNP, PRRT2, PTF1A, RARS2, RUBCN, RNF170, RNF216, SACS, SAR1B, SCN2A, SEPSECS, SETX, SIL1, SLC1A3, SLC2A1, SLC9A6, SNX14, SPG7, SPTBN2, SRD5A3, STUB1, SYNE1, SYT14, TDP1, TGM6, TENM4, TMEM240, TPP1, TSEN2, TSEN54, TTBK2, TTC19, TTPA, TUBB4A, T |
|
Câncer de Prostata |
Painel por Sequenciamento de Próxima Geração |
ATM, BRCA1, BRCA2, CHEK2, NBN, TP53 |
|
Carcinoma Papilífero da Tireóide |
Painel por Sequenciamento de Próxima Geração |
APC, ATM, BRAF, BRCA1, BRCA2, CHEK2, DICER1, DIRC3, FOXE1, GNAS, HABP2, HRAS, MEN1, MINPP1, MSH2, MSH6, MYH9, NDUFA13, NKX2-1, PIK3CA, PRKAR1A, PTEN, PTCSC2, PTCSC3, RASAL1, SRRM2, SRGAP1, SDHB, SDHD, SEC23B, SLC5A5, TG, WRN, XRCC1 |
|
Instabilidade Cromossômica, Síndrome |
Painel por Sequenciamento de Próxima Geração |
ATM, BLM, ERCC6, ERCC8, MRE11A, NBN, RECQL4, WRN |
|
Painel para Detecção de Portadores Assintomáticos de Doenças Genéticas Frequentes em Judeus |
Painel por Sequenciamento de Próxima Geração |
ABCB11, ABCC8, ABCD1, ACAD9, ACADM, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADGRG1, AGA, AGL, AGPS, AGXT, AIRE, ALDH3A2, ALDOB, ALG6, ALMS1, ALPL, AMT, AQP2, ARG1, ARSA, ARSB, ASL, ASNS, ASPA, ASS1, ATM, ATP6V1B1, ATP7A, ATP7B, ATRX, BBS1, BBS10, BBS12, BBS2, BCKDHA, BCKDHB, BCS1L, BLM, BSND, CAPN3, CBS, CDH23, CEP290, CERKL, CFTR, CHM, CHRNE, CIITA, CLN3, CLN5, CLN6, CLN8, CLRN1, CNGB3, COL27A1, COL4A3, COL4A4, COL4A5, COL7A1, CPS1, CPT1A, CPT2, CRB1, CTNS, CTSK, CYBA, CYBB, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP27A1, DBT, DCLRE1C, DHCR7, DHDDS, DLD, DMD, DNAH5, DNAI1, DNAI2, DYSF, EDA, EIF2B5, ELP1, EMD, ERCC6, ERCC8, ESCO2, ETFA, ETFDH, ETHE1, EVC, EVC2, EYS, F9, FAH, FAM161A, FANCA, FANCC, FANCG, FH, FKRP, FKTN, FMR1, G6PC, GAA, GALC, GALK1, GALT, GAMT, GBA, GBE1, GCDH, GFM1, GJB1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPTAB, GNPTG, GNS, GRHPR, HADHA, HAX1, HBA1, HBA2, HBB, HEXA, HEXB, HGSNAT, HJV, HLCS, HMGCL, HOGA1, HPS1, HPS3, HSD17B4, HSD3B2, HYAL1, HYLS1, IDS, IDUA, IL2RG, IVD, KCNJ11, LAMA2, LAMA3 |
|
Câncer de Mama, Predisposição Hereditária |
Painel por Sequenciamento de Próxima Geração |
AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDC73, CDH1, CHEK2, DICER1, EPCAM, FAM175A, FANCC, MLH, MRE11, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PIK3CA, PMS2, POLD, PTEN, RAD50, RAD51C, RAD51D, RINT1, SDHB, SDHD, SMARCA4, STK11, TP53, XRCC2 |
|
Doenças Neuromusculares |
Painel por Sequenciamento de Próxima Geração |
AARS, ABCD1, AFG3L2, ANO5, APTX, ASPA, ATL1, ATM, ATP7A, CACNA1S, CAPN3, CAV3, CLCN1, CP, CYP7B1, DAG1, DES, DMD, DNAJB6, DNM2, DYSF, EGR2, EMD, FGD4, FHL1, FIG4, FKRP, FKTN, FLNC, FUS, FXN, GARS, GDAP1, GJB1, GJB3, HSPB1, HSPB8, KIF5A, L1CAM, LAMP2, LITAF, LMNA, LRSAM1, MED25, MFN2, MPZ, MSTN, MTM1, MTMR2, MYOT, NDRG1, NEFL, NIPA1, NOTCH3, PABPN1, PMP22, POMGNT1, POMT1, POMT2, PRPS1, PRX, PYGM, RAB7A, REEP1, SBF2, SCN4A, SCO2, SETX, SGCA, SGCB, SGCD, SGCG, SOD1, SPAST, SPG11, SPG7, TARDBP, TCAP, TRIM32, TRPV4, VAPB |
|
Predisposição ao Câncer |
Painel por Sequenciamento de Próxima Geração |
APC, ATM, BARD1, BLM, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EGFR, EPCAM, FANCC, MEN1, MET, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, NF2, PALB2, PIK3CA, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, RB1, RECQL, RET, STK11, TP53, WT1, VHL |
|
Câncer de Pâncreas Hereditario |
Painel por Sequenciamento de Próxima Geração |
APC, ATM, BRCA2, BRCA1, BMPR1A, CHEK2, CDKN2A, EPCAM, MEN1, MLH1, MSH2, MSH6, MUTYH, PMS2, PALB2, STK11, SMAD4, TP53, VHL |
|
Neoplasia de Mama e Cólon |
Análise de Deleção/Duplicação |
ATM |
|
Neuropatia Metabólica Sindrômica |
Painel por Sequenciamento de Próxima Geração |
ABCD1, ARSA, ATM, CTDP1, CYP27A1, FBLN5, GALC, GAN, GBE1, GJB3, GLA, HMBS, L1CAM, PHYH, PRPS1, TTR, TUBB3, TYMP, XPC |
|
Neuropatia Periférica |
Painel por Sequenciamento de Próxima Geração |
AARS, ABCD1, ARHGEF10, ARSA, ATL1, ATM, ATP7A, BICD2, BSCL2, CCT5, CTDP1, CYP27A1, CYP7B1, DCTN1, DCAF8, DHTKD1, DNAJB2, DNM2, DNMT1, DST, DYNC1H1, EGR2, FAM134B, FBLN5, FGD4, FIG4, GALC, GAN, GARS1, GBE1, GDAP1, GJB1, GJB3, GLA, GNB4, HARS, HINT1, HINT2, HK1, HMBS, HSN2, HSPB1, HSPB3, HSPB8, HSPD1, IGHMBP2, IKBKAP, INF2, KARS, KIAA0196, KIF1A, KIF1B, KIF5A, L1CAM, LITAF, LMNA, LRSAM1, MED25, MFN2, MPZ, MTMR2, NDRG1, NEFL, NGF, NIPA1, NTRK1, PDK3, PHYH, PLEKHG5, PLP1, PMP22, PRPS1, PRX, RAB7A, REEP1, RTN2, SBF2, SCN9A, SETX, SH3TC2, SLC12A6, SLC16A2, SLC5A7, SOD1, SPAST, SPG11, SPG20, SPG21, SPG7, SPTLC1, SPTLC2, SPTLC3, TFG, TRIM2, TRPV4, TTR, TUBB3, TYMP, WNK1, XPC, YARS, ZFYVE26, ZFYVE27, ABHD12, AIFM1, ATP1A1, BAG3, CNTNAP1, COA7, DCTN2, DGAT2, DRP2, MARS, MCM3AP, MME, MORC2, MPV17, NAGLU, NEFH, PMP2, PTRH2, RAB7, SBF1, SCO2, SGPL1, SIGMAR1, VCP, WARS |
|
Neuropatia, Painel Expandido |
Painel por Sequenciamento de Próxima Geração |
AAAS, AARS, ABCA1, ABHD12, ACTA1, ADAR, AGRN, AIFM1, ALG14, ALG2, ALS2, AMACR, ANG, ANO5, ARHGEF10, ASAH1, ASCC1, ATL1, ATL3, ATM, ATP7A, B3GALNT2, B4GAT1, BAG3, BICD2, BIN1, BSCL2, C12ORF65, CAPN3, CASQ1, CCDC78, CCT5, CFL2, CHAT, CHCHD10, CHKB, CHMP2B, CHRNA1, CHRNB1, CHRND, CHRNE, CLP1, CNTN1, COL12A1, COL13A1, COL6A1, COL6A2, COL6A3, COLQ, COX10, COX6A1, CTDP1, CYP27A1, DAG1, DCAF8, DCTN1, DES, DGAT2, DHTKD1, DMD, DNAJB2, DNAJB5, DNM2, DNMT1, DOK7, DOLK, DPAGT1, DPM1, DPM2, DPM3, DST, DYNC1H1, DYSF, EGR2, EMD, EPG5, EXOSC3, EXOSC8, FAM126A, FAM134B, FBLN5, FBXO38, FGD4, FHL1, FIG4, FKBP14, FKRP, FKTN, FUS, FXN, GAA, GALC, GAN, GARS, GBA, GBE1, GDAP1, GFPT1, GJB1, GLA, GMPPB, GNB4, GSN, GYG1, HADHA, HADHB, HARS, HEXA, HINT1, HK1, HMBS, HNRNPA1, HNRNPA2B1, HNRNPDL, HSPB1, HSPB3, HSPB8, IFRD1, IGHMBP2, IKBKAP, INF2, ISPD, ITGA7, KARS, KBTBD13, KIF1A, KIF5A, KLHL13, KLHL40, KY, LAMA2, LAMB2, LAMP2, LARGE1, LAS1L, LIMS2, LITAF, LMNA, LMOD3, LRP4, LRSAM1, MARS, MATR3, MED25, MEGF10, MFN2, MICAL1, MICU1, MORC2 |
|
Distonia, Discinesia |
Painel por Sequenciamento de Próxima Geração |
ACY1, ADCY5, ANO3, ATM, ATP13A2, ATP1A3, CACNA1B, CIZ1, COL6A3, DLAT, GCDH, GCH1, GNAL, HPCA, KCNMA1, KCTD17, MR1, PDHA1, PDHX, PLA2G6, PNKD, PRKRA, PRRT2, RELN, SCN8A, SGCE, SLC16A2, SLC2A1, SLC30A10, SLC6A3, SPR, SUCLA2, TAF1, TH, THAP1, TOR1A, TUBB4A |
|
Predisposição ao Câncer de Mama e/ou Ovário |
Painel por Sequenciamento de Próxima Geração |
ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, MLH1, MSH2, MSH6, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53 |
|
Câncer, Predisposição Hereditária |
Painel por Sequenciamento de Próxima Geração |
ABCB1, ABCC2, ABCC4, ABCG2, ABL1, ABL2, ACVR1, ACVR1B, AKT1, AKT2, AKT3, ALK, ALOX12B, AMER1, ANKRD26, APC, AR, ARAF, ARFRP1, ARID1A, ARID1B, ARID2, ASXL1, ASXL2, ATM, ATR, ATRX, AURKA, AURKB, AXIN1, AXL, B2M, BAP1, BARD1, BCL10, BCL2, BCL2L1, BCL2L11, BCL2L2, BCL6, BCOR, BCORL1, BLM, BRAF, BRCA1, BRCA2, BRD3, BRD4, BRIP1, BTG1, BTG2, BTK, C11ORF30, CALR, CARD11, CASP8, CBFB, CBL, CCND1, CCND2, CCND3, CCNE1, CD22, CD274, CD70, CD79A, CD79B, CDC73, CDH1, CDK12, CDK4, CDK6, CDK8, CDKN1A, CDKN1B, CDKN2A, CDKN2B, CDKN2C, CEBPA, CHD2, CHD4, CHEK1, CHEK2, CIC, CREBBP, CRKL, CRLF2, CSF1R, CSF3R, CTCF, CTLA4, CTNNA1, CTNNB1, CUL3, CUL4A, CUX1, CXCR4, CYLD, CYP17A1, DAXX, DDR1, DDR2, DDX41, DICER1, DIS3, DNMT3A, DNMT3B, DOT1L, EED, EGFR, EIF1AX, EIF4A2, ELANE, EP300, EPCAM, EPHA3, EPHA5, EPHA7, EPHB1, EPHB4, ERBB2, ERBB3, ERBB4, ERCC1, ERCC2, ERCC3, ERCC4, ERG, ERRFI1, ESR1, ETNK1, ETV1, ETV6, EZH2, FAM175A, FAM46C, FANCA, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FAS, FAT1, FBXW7, FGF10, FGF12 |
|
Câncer Cerebral Hereditário |
Painel por Sequenciamento de Próxima Geração + Análise de Deleção/Duplicação |
ALK, APC, ATM, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PALB2, PHOX2B, PMS2, PTCH1, SUFU, TP53, VHL |
|
Câncer, Mutações Conhecidas |
Painel por Sequenciamento de Próxima Geração |
ABL1, AKT1, ALK, APC, ATM, BRAF, CDH1, CDKN2A, CSF1R, CTNNB1, EGFR, ERBB2, ERBB4, EZF2, FBXW7, FGFR1, FGFR2, FGFR3, FLT3, GNA11, GNAQ, GNAS, HNF1A, HRAS, IDH1, IDH2, JAK2, JAK3, KDR, KIT, KRAS, MET, MLH1, MPL, NOTCH1, NPM1, NRAS, PDGFRA, PIK3CA, PTEN, PTPN11, RB1, RET, SMAD4, SMARCB1, SMO, SRC, STK11 |
|
Câncer Hereditário |
Painel por Sequenciamento de Próxima Geração |
APC, ATM, BAP1, BARD1, BRIP1, BMPR1A, BRCA1, BRCA2, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53 |
|
Predisposição ao Câncer de Mama e/ou Ovário em Familias com BRCA Normal |
Painel por Sequenciamento de Próxima Geração |
ATM, BRIP1, CDH1, CHEK2, MLH1, MSH2, MSH6, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53 |
|
Ataxia Telangiectasia |
Sequenciamento Completo do Gene |
ATM |
