ClinVar Miner

List of variants reported as benign for breast-ovarian cancer, familial, susceptibility to, 1 by Myriad Genetics, Inc.

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_007294.4(BRCA1):c.-19-3A>G rs273898669 0.00004
NM_007294.4(BRCA1):c.2286A>T (p.Arg762Ser) rs273898682 0.00004
NM_007294.4(BRCA1):c.1228G>A (p.Ala410Thr) rs779974365 0.00001
NM_007294.4(BRCA1):c.5194-16G>A rs368058346 0.00001
NM_007294.4(BRCA1):c.799T>C (p.Ser267Pro) rs587781496 0.00001
NM_007294.4(BRCA1):c.1310A>G (p.His437Arg) rs80357255
NM_007294.4(BRCA1):c.189A>T (p.Leu63Phe) rs80356956
NM_007294.4(BRCA1):c.332A>C (p.Glu111Ala) rs80357312
NM_007294.4(BRCA1):c.3410T>C (p.Met1137Thr) rs80357297
NM_007294.4(BRCA1):c.4657T>A (p.Leu1553Met) rs80357431
NM_007294.4(BRCA1):c.575A>G (p.Asn192Ser) rs2054178411
NM_007294.4(BRCA1):c.81-20C>T rs80358039

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