ClinVar Miner

List of variants in gene SLC12A3 reported as uncertain significance for not specified

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001126108.2(SLC12A3):c.363G>C (p.Glu121Asp) rs146632606 0.00102
NM_001126108.2(SLC12A3):c.2285+8G>A rs199854613 0.00061
NM_001126108.2(SLC12A3):c.2470T>A (p.Ser824Thr) rs146845953 0.00038
NM_001126108.2(SLC12A3):c.1709C>T (p.Ala570Val) rs201130736 0.00019
NM_001126108.2(SLC12A3):c.2920G>A (p.Val974Ile) rs373092349 0.00009
NM_001126108.2(SLC12A3):c.1258G>A (p.Ala420Thr) rs137970015 0.00001
NM_001126108.2(SLC12A3):c.1045C>G (p.Pro349Ala)
NM_001126108.2(SLC12A3):c.1160T>C (p.Leu387Pro)
NM_001126108.2(SLC12A3):c.1247G>C (p.Cys416Ser) rs1429832884
NM_001126108.2(SLC12A3):c.1373C>T (p.Thr458Met)
NM_001126108.2(SLC12A3):c.1568C>T (p.Ala523Val)
NM_001126108.2(SLC12A3):c.205C>A (p.His69Asn)
NM_001126108.2(SLC12A3):c.2720+8C>T rs957373573
NM_001126108.2(SLC12A3):c.450T>G (p.Ile150Met) rs143714318
NM_001126108.2(SLC12A3):c.509T>A (p.Leu170Gln)
NM_001126108.2(SLC12A3):c.581C>T (p.Thr194Ile)
NM_001126108.2(SLC12A3):c.781C>T (p.Arg261Cys)
NM_001126108.2(SLC12A3):c.793G>A (p.Val265Met)
NM_001126108.2(SLC12A3):c.941C>T (p.Ser314Phe) rs1555499734

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