ClinVar Miner

List of variants in gene combination GH-LCR, SCN4A reported as likely benign for Hyperkalemic Periodic Paralysis Type 1

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Total variants: 28
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HGVS dbSNP
NM_000334.4(SCN4A):c.2188G>A (p.Val730Met) rs113462659
NM_000334.4(SCN4A):c.2208C>T (p.Asp736=) rs751675273
NM_000334.4(SCN4A):c.2220G>A (p.Pro740=) rs368278422
NM_000334.4(SCN4A):c.2223C>T (p.Arg741=) rs1041781133
NM_000334.4(SCN4A):c.2340C>T (p.Thr780=) rs375349902
NM_000334.4(SCN4A):c.2448T>C (p.Asp816=) rs150307926
NM_000334.4(SCN4A):c.2574C>T (p.Leu858=) rs184107335
NM_000334.4(SCN4A):c.2623C>T (p.Pro875Ser) rs201148948
NM_000334.4(SCN4A):c.2697G>A (p.Leu899=) rs199827271
NM_000334.4(SCN4A):c.2889C>A (p.Ser963=) rs757881584
NM_000334.4(SCN4A):c.2995G>A (p.Val999Met) rs377277110
NM_000334.4(SCN4A):c.3001C>T (p.Arg1001Cys) rs199713025
NM_000334.4(SCN4A):c.3039T>C (p.Arg1013=) rs1319435457
NM_000334.4(SCN4A):c.3099C>T (p.Phe1033=) rs753862870
NM_000334.4(SCN4A):c.3312C>T (p.Ile1104=) rs779189351
NM_000334.4(SCN4A):c.3357C>T (p.Tyr1119=) rs903219930
NM_000334.4(SCN4A):c.3360G>A (p.Ser1120=) rs377187913
NM_000334.4(SCN4A):c.4416G>A (p.Leu1472=) rs758113478
NM_000334.4(SCN4A):c.4690G>A (p.Val1564Ile) rs202106192
NM_000334.4(SCN4A):c.4719C>T (p.Ile1573=) rs562551941
NM_000334.4(SCN4A):c.4886C>T (p.Pro1629Leu) rs202102815
NM_000334.4(SCN4A):c.4890C>T (p.Asp1630=) rs781276397
NM_000334.4(SCN4A):c.5037C>T (p.Ile1679=) rs372002602
NM_000334.4(SCN4A):c.5148G>A (p.Glu1716=) rs1244264430
NM_000334.4(SCN4A):c.5181G>A (p.Glu1727=) rs368263333
NM_000334.4(SCN4A):c.5218C>A (p.Arg1740=) rs373804267
NM_000334.4(SCN4A):c.5343C>T (p.Gly1781=) rs745441690
NM_000334.4(SCN4A):c.5424G>A (p.Met1808Ile) rs201375413

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