ClinVar Miner

List of variants in gene ABCC6 reported as uncertain significance

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Total variants: 33
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HGVS dbSNP
GRCh37/hg19 16p13.11(chr16:16246164-16261251)x1
GRCh37/hg19 16p13.11(chr16:16247252-16258276)x1
GRCh37/hg19 16p13.11(chr16:16247818-16258276)x1
NM_001171.5(ABCC6):c.1094T>C (p.Leu365Pro) rs1064794607
NM_001171.5(ABCC6):c.1112T>C (p.Met371Thr) rs756614582
NM_001171.5(ABCC6):c.1171A>G (p.Arg391Gly) rs72653762
NM_001171.5(ABCC6):c.1263C>T (p.Thr421=) rs114179357
NM_001171.5(ABCC6):c.1424A>T (p.His475Leu) rs151187637
NM_001171.5(ABCC6):c.1639G>A (p.Ala547Thr) rs56877937
NM_001171.5(ABCC6):c.1765_1766insCTGC (p.His589fs) rs1567511016
NM_001171.5(ABCC6):c.2059G>A (p.Val687Met) rs368806440
NM_001171.5(ABCC6):c.2247+22T>G rs72664298
NM_001171.5(ABCC6):c.2293C>G (p.Arg765Gly) rs776513864
NM_001171.5(ABCC6):c.2359G>A (p.Val787Ile) rs72653792
NM_001171.5(ABCC6):c.2393C>T (p.Pro798Leu) rs142223793
NM_001171.5(ABCC6):c.2428G>A (p.Val810Met) rs72653795
NM_001171.5(ABCC6):c.2782G>A (p.Gly928Ser) rs142470921
NM_001171.5(ABCC6):c.2848G>A (p.Ala950Thr) rs72657689
NM_001171.5(ABCC6):c.2935G>C (p.Gly979Arg) rs569941928
NM_001171.5(ABCC6):c.2965G>A (p.Gly989Arg) rs529676674
NM_001171.5(ABCC6):c.3557C>A (p.Ala1186Asp) rs149460452
NM_001171.5(ABCC6):c.3691G>A (p.Val1231Met) rs141728905
NM_001171.5(ABCC6):c.3739C>T (p.Pro1247Ser) rs199694536
NM_001171.5(ABCC6):c.3802C>T (p.Arg1268Trp) rs368379895
NM_001171.5(ABCC6):c.3941G>A (p.Arg1314Gln) rs63751086
NM_001171.5(ABCC6):c.4002G>C (p.Gly1334=) rs139128550
NM_001171.5(ABCC6):c.4249C>G (p.Leu1417Val) rs1567460585
NM_001171.5(ABCC6):c.4253G>A (p.Arg1418Gln) rs63751262
NM_001171.5(ABCC6):c.4375C>T (p.Arg1459Cys) rs72547524
NM_001171.5(ABCC6):c.496C>T (p.Arg166Cys) rs201766106
NM_001171.5(ABCC6):c.560C>T (p.Ala187Val) rs561266462
NM_001171.5(ABCC6):c.742C>T (p.Leu248Phe) rs72653756
NM_001171.5(ABCC6):c.790C>T (p.Arg264Trp)

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