ClinVar Miner

List of variants reported as uncertain significance for breast-ovarian cancer, familial, susceptibility to, 4 by Counsyl

Included ClinVar conditions (1):
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Total variants: 23
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HGVS dbSNP
NM_002878.3(RAD51D):c.131G>A (p.Gly44Asp) rs374730714
NM_002878.3(RAD51D):c.137C>G (p.Ser46Cys) rs587780102
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.196G>A (p.Val66Met) rs56026142
NM_002878.3(RAD51D):c.26G>C (p.Cys9Ser) rs140825795
NM_002878.3(RAD51D):c.286G>T (p.Gly96Cys) rs762951311
NM_002878.3(RAD51D):c.339A>C (p.Lys113Asn) rs786202507
NM_002878.3(RAD51D):c.349T>A (p.Cys117Ser) rs786201358
NM_002878.3(RAD51D):c.394G>A (p.Val132Ile) rs201141245
NM_002878.3(RAD51D):c.413A>G (p.Asn138Ser) rs201676898
NM_002878.3(RAD51D):c.433C>T (p.Arg145Cys) rs755173206
NM_002878.3(RAD51D):c.53A>G (p.Gln18Arg) rs546225564
NM_002878.3(RAD51D):c.568G>A (p.Ala190Thr) rs80116829
NM_002878.3(RAD51D):c.629C>T (p.Ala210Val) rs376855484
NM_002878.3(RAD51D):c.715C>T (p.Arg239Trp) rs770250516
NM_002878.3(RAD51D):c.716G>A (p.Arg239Gln) rs780921112
NM_002878.3(RAD51D):c.739-3C>T rs1235042092
NM_002878.3(RAD51D):c.785C>T (p.Pro262Leu) rs730881950
NM_002878.3(RAD51D):c.796C>T (p.Arg266Cys) rs587781813
NM_002878.3(RAD51D):c.904-3C>T rs45478491
NM_002878.3(RAD51D):c.932T>A (p.Ile311Asn) rs145309168
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595
NM_017559.2(FNDC8):c.-1802_-1798del5 rs761104531

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