ClinVar Miner

List of variants in gene KCNQ1 reported as likely benign for not provided

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Total variants: 20
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HGVS dbSNP
NM_000218.2(KCNQ1):c.160_168dup (p.Ile54_Pro56dup) rs397515877
NM_000218.2(KCNQ1):c.328G>A (p.Val110Ile) rs199472677
NM_181798.1(KCNQ1):c.1413+102C>G
NM_181798.1(KCNQ1):c.1470C>T (p.Leu490=) rs962199389
NM_181798.1(KCNQ1):c.1557C>T (p.Gly519=)
NM_181798.1(KCNQ1):c.189G>T (p.Arg63=)
NM_181798.1(KCNQ1):c.203G>A (p.Arg68Gln) rs138362632
NM_181798.1(KCNQ1):c.238G>A (p.Val80Met) rs75813654
NM_181798.1(KCNQ1):c.400-107G>A
NM_181798.1(KCNQ1):c.400-117G>A
NM_181798.1(KCNQ1):c.5+289_5+292del
NM_181798.1(KCNQ1):c.5+293A>G
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.798G>T (p.Lys266Asn) rs12720457
NM_181798.1(KCNQ1):c.870+277A>G
NM_181798.1(KCNQ1):c.871-311C>T
NM_181798.1(KCNQ1):c.900A>G (p.Lys300=) rs763197403
NM_181798.1(KCNQ1):c.942C>T (p.Pro314=) rs145452045
NM_181798.1(KCNQ1):c.96+4C>T
NM_181798.1(KCNQ1):c.962C>G (p.Pro321Arg) rs12720449

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