ClinVar Miner

List of variants in gene WRN reported as pathogenic for not provided

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_000553.6(WRN):c.1105C>T (p.Arg369Ter) rs17847577 0.00033
NM_000553.6(WRN):c.2665C>T (p.Arg889Ter) rs774765029 0.00002
NM_000553.6(WRN):c.3130dup (p.Thr1044fs) rs1563376595 0.00001
NM_000553.6(WRN):c.1165del (p.Arg389fs) rs878854131
NM_000553.6(WRN):c.171C>A (p.Tyr57Ter) rs373806031
NM_000553.6(WRN):c.1726G>T (p.Gly576Ter) rs1396973081
NM_000553.6(WRN):c.2704del (p.Tyr902fs) rs1801847909
NM_000553.6(WRN):c.2900dup (p.Leu967fs) rs1554530901
NM_000553.6(WRN):c.561A>G (p.Lys187=) rs775802030

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