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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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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.2959C>T (p.Arg987Ter)	rs747319628	0.00003
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.1940del (p.Cys646_Ser647insTer)
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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