List of variants in gene WRN reported as benign by Illumina Clinical Services Laboratory,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: 21

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HGVS	dbSNP
NM_000553.4(WRN):c.-278G>C	rs11574157
NM_000553.4(WRN):c.-408C>T	rs11574156
NM_000553.4(WRN):c.-618C>G	rs7017069
NM_000553.6(WRN):c.*570A>G	rs11574415
NM_000553.6(WRN):c.-163C>G	rs11574160
NM_000553.6(WRN):c.-213G>A	rs11574158
NM_000553.6(WRN):c.1155G>A (p.Glu385=)	rs2230010
NM_000553.6(WRN):c.1161G>A (p.Met387Ile)	rs1800391
NM_000553.6(WRN):c.1577-3C>A	rs3087409
NM_000553.6(WRN):c.1982-5del	rs397723919
NM_000553.6(WRN):c.2361G>T (p.Leu787=)	rs1800392
NM_000553.6(WRN):c.3138+6C>T	rs3024239
NM_000553.6(WRN):c.3138+7G>A	rs2737335
NM_000553.6(WRN):c.3222G>T (p.Leu1074Phe)	rs1801195
NM_000553.6(WRN):c.3236C>T (p.Ser1079Leu)	rs3087414
NM_000553.6(WRN):c.3384-3T>C	rs3087424
NM_000553.6(WRN):c.340G>A (p.Val114Ile)	rs2230009
NM_000553.6(WRN):c.4083C>T (p.Ser1361=)	rs1801196
NM_000553.6(WRN):c.4099T>C (p.Cys1367Arg)	rs1346044
NM_000553.6(WRN):c.513C>T (p.Cys171=)	rs1800389
NM_000553.6(WRN):c.970A>G (p.Thr324Ala)	rs1800390

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