SNP Directory

450,817 genetic variants in our database.

All (450,817) Health Risk (400,964) Other (47,777) Drug Response (1,898) Trait (128) Protective (50)
RSID Gene Category Clinical Significance Conditions
RS397507356 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507357 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507358 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary breast ovarian cancer syndrome
RS397507359 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507360 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507361 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary breast ovarian cancer syndrome, Hereditary cancer-predisposing syndrome
RS397507362 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507363 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507364 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507365 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507366 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507367 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507368 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507369 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507370 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507371 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507373 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507374 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507375 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507379 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary breast ovarian cancer syndrome
RS397507382 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507383 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507385 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507386 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507387 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507388 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507389 BRCA2 Health Risk Likely pathogenic Breast-ovarian cancer, familial
RS397507390 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507393 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507394 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary breast ovarian cancer syndrome
RS397507395 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507396 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507397 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary breast ovarian cancer syndrome
RS397507399 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507400 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507402 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507403 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507404 BRCA2 Health Risk Pathogenic Fanconi anemia complementation group D1, Breast-ovarian cancer
RS397507406 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507407 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507409 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507410 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507411 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507412 BRCA2 Health Risk Likely pathogenic Breast-ovarian cancer, familial
RS397507413 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507414 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507416 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507417 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507418 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507419 BRCA2 Health Risk Pathogenic/Likely pathogenic Breast-ovarian cancer, familial
RS397507422 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507423 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507424 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507425 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507426 BRCA2 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary breast ovarian cancer syndrome
RS397507427 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507428 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507430 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507435 BRCA2 Health Risk Conflicting classifications of pathogenicity Breast-ovarian cancer, familial
RS397507437 BRCA2 Health Risk Pathogenic Breast-ovarian cancer, familial
RS397507438 MPV17 Health Risk Pathogenic Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
RS397507439 PRSS1 Health Risk Pathogenic Hereditary pancreatitis, Hereditary pancreatitis
RS397507440 PRSS1 Health Risk Conflicting classifications of pathogenicity Hereditary pancreatitis, Hereditary pancreatitis
RS397507445 PCCB Health Risk Pathogenic/Likely pathogenic Propionic acidemia, Inborn genetic diseases
RS397507447 GNPTAB Health Risk Pathogenic Mucolipidosis type II, Pseudo-Hurler polydystrophy
RS397507448 GNPTAB Health Risk Pathogenic Mucolipidosis type II, Pseudo-Hurler polydystrophy
RS397507457 BRAF Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS397507458 BRAF Health Risk Conflicting classifications of pathogenicity RASopathy, Noonan syndrome
RS397507464 BRAF Health Risk Conflicting classifications of pathogenicity RASopathy, RASopathy
RS397507465 BRAF Health Risk Pathogenic Cardio-facio-cutaneous syndrome, RASopathy
RS397507466 BRAF Health Risk Pathogenic Cardio-facio-cutaneous syndrome, LEOPARD syndrome 3
RS397507467 BRAF Health Risk Conflicting classifications of pathogenicity Noonan syndrome and Noonan-related syndrome, RASopathy
RS397507469 BRAF Health Risk Pathogenic/Likely pathogenic Noonan syndrome, Cardio-facio-cutaneous syndrome
RS397507470 BRAF Health Risk Pathogenic/Likely pathogenic RASopathy, RASopathy
RS397507473 BRAF Health Risk Pathogenic/Likely pathogenic Cardio-facio-cutaneous syndrome, RASopathy
RS397507474 BRAF Health Risk Pathogenic/Likely pathogenic Cardio-facio-cutaneous syndrome, Cardio-facio-cutaneous syndrome
RS397507475 BRAF Health Risk Pathogenic Cardio-facio-cutaneous syndrome, Noonan syndrome and Noonan-related syndrome
RS397507476 BRAF Health Risk Pathogenic Cardio-facio-cutaneous syndrome, Cardiofaciocutaneous syndrome 1
RS397507477 BRAF Health Risk Pathogenic Noonan syndrome, RASopathy
RS397507478 BRAF Health Risk Conflicting classifications of pathogenicity Cardiofaciocutaneous syndrome 1, Noonan syndrome 7
RS397507479 BRAF Health Risk Likely pathogenic Cardio-facio-cutaneous syndrome, RASopathy
RS397507480 BRAF Health Risk Likely pathogenic Cardio-facio-cutaneous syndrome, Noonan syndrome and Noonan-related syndrome
RS397507481 BRAF Health Risk Pathogenic Cardiofaciocutaneous syndrome 1, Cardio-facio-cutaneous syndrome
RS397507482 BRAF Health Risk Likely pathogenic Cardiofaciocutaneous syndrome 1, Cardiofaciocutaneous syndrome 1
RS397507483 BRAF Health Risk Pathogenic RASopathy, Cardio-facio-cutaneous syndrome
RS397507484 BRAF Health Risk Pathogenic RASopathy, Cardio-facio-cutaneous syndrome
RS397507486 BRAF Health Risk Pathogenic Cardiofaciocutaneous syndrome 1, Cardiofaciocutaneous syndrome 1
RS397507489 CBL Health Risk Pathogenic CBL-related disorder, CBL-related disorder
RS397507490 CBL Health Risk Pathogenic RASopathy, RASopathy
RS397507491 CBL Health Risk Pathogenic —
RS397507492 CBL Health Risk Conflicting classifications of pathogenicity RASopathy, CBL-related disorder
RS397507493 CBL Health Risk Pathogenic RASopathy, RASopathy
RS397507497 CBL Health Risk Conflicting classifications of pathogenicity RASopathy, RASopathy
RS397507501 PTPN11 Health Risk Pathogenic Noonan syndrome, RASopathy
RS397507502 PTPN11 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS397507503 PTPN11 Health Risk Pathogenic Noonan syndrome, RASopathy
RS397507504 PTPN11 Health Risk Pathogenic Noonan syndrome, RASopathy
RS397507505 PTPN11 Health Risk Pathogenic/Likely pathogenic Noonan syndrome, RASopathy
RS397507506 PTPN11 Health Risk Pathogenic/Likely pathogenic Noonan syndrome, Noonan syndrome 3
RS397507507 PTPN11 Health Risk Conflicting classifications of pathogenicity Noonan syndrome, RASopathy
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