ClinVar Miner

List of variants in gene WRN reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NC_000008.11:g.31033419G>C
NM_000553.6(WRN):c.*194C>T rs11574411
NM_000553.6(WRN):c.*415C>G
NM_000553.6(WRN):c.1725T>C (p.Tyr575=) rs13438802
NM_000553.6(WRN):c.1788T>C (p.Ser596=) rs13438803
NM_000553.6(WRN):c.1882C>G (p.Leu628Val) rs77969734
NM_000553.6(WRN):c.1953C>T (p.Gly651=) rs11574263
NM_000553.6(WRN):c.2241T>G (p.Leu747=) rs2230011
NM_000553.6(WRN):c.2500C>T (p.Arg834Cys) rs3087425
NM_000553.6(WRN):c.3237G>A (p.Ser1079=) rs11574345
NM_000553.6(WRN):c.3422C>T (p.Ser1141Leu) rs139323683
NM_000553.6(WRN):c.4015G>A (p.Val1339Ile) rs11574395
NM_000553.6(WRN):c.4216C>T (p.Arg1406Ter) rs11574410

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