ClinVar Miner

List of variants in gene LDB3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.1231+30C>G rs11597201 0.05370
NM_007078.3(LDB3):c.689+10G>A rs45563234 0.00125
NM_007078.3(LDB3):c.1653C>T (p.Cys551=) rs45581435 0.00096
NM_007078.3(LDB3):c.993G>A (p.Ala331=) rs140347820 0.00095
NM_007078.3(LDB3):c.1111G>A (p.Ala371Thr) rs45539535 0.00054
NM_007078.3(LDB3):c.1045T>A (p.Ser349Thr) rs147042608 0.00051
NM_007078.3(LDB3):c.664G>A (p.Ala222Thr) rs139922045 0.00036
NM_007078.3(LDB3):c.732C>T (p.Pro244=) rs144509718 0.00034
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala) rs138251566 0.00026
NM_007078.3(LDB3):c.492G>T (p.Pro164=) rs368407147 0.00015
NM_007078.3(LDB3):c.1697T>G (p.Met566Arg) rs566463138 0.00006
NM_007078.3(LDB3):c.468C>T (p.Ala156=) rs374233873 0.00002
NM_007078.3(LDB3):c.322-20C>T rs199536065 0.00001
NM_007078.3(LDB3):c.550A>G (p.Lys184Glu) rs774886148 0.00001
NM_007078.3(LDB3):c.1167C>T (p.Ala389=) rs768844187
NM_007078.3(LDB3):c.1317C>T (p.Pro439=) rs397517208
NM_007078.3(LDB3):c.1836G>A (p.Lys612=) rs886038406
NM_007078.3(LDB3):c.2103T>C (p.His701=)
NM_007078.3(LDB3):c.408G>A (p.Pro136=) rs375626151
NM_007078.3(LDB3):c.447C>G (p.Pro149=)
NM_007078.3(LDB3):c.465C>T (p.Leu155=) rs45516997
NM_007078.3(LDB3):c.896+6669TC[8]

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