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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.2241T>G (p.Leu747=)	rs2230011	0.00921
NM_000553.6(WRN):c.1953C>T (p.Gly651=)	rs11574263	0.00627
NM_000553.6(WRN):c.1725T>C (p.Tyr575=)	rs13438802	0.00516
NM_000553.6(WRN):c.1788T>C (p.Ser596=)	rs13438803	0.00512
NM_000553.6(WRN):c.*415C>G	rs11574412	0.00435
NM_000553.6(WRN):c.4015G>A (p.Val1339Ile)	rs11574395	0.00418
NM_000553.6(WRN):c.*194C>T	rs11574411	0.00413
NM_000553.6(WRN):c.2500C>T (p.Arg834Cys)	rs3087425	0.00089
NM_000553.6(WRN):c.3237G>A (p.Ser1079=)	rs11574345	0.00069
NM_000553.6(WRN):c.3422C>T (p.Ser1141Leu)	rs139323683	0.00052
NM_000553.6(WRN):c.1882C>G (p.Leu628Val)	rs77969734	0.00050
NM_000553.5(WRN):c.-631G>C	rs10112017

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