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

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

Total variants: 6

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HGVS	dbSNP
NM_000553.4(WRN):c.1982-5delT	rs397723919
NM_000553.4(WRN):c.2361G>T (p.Leu787=)	rs1800392
NM_000553.4(WRN):c.3138+6C>T	rs3024239
NM_000553.4(WRN):c.3138+7G>A	rs2737335
NM_000553.4(WRN):c.3222G>T (p.Leu1074Phe)	rs1801195
NM_000553.5(WRN):c.513C>T (p.Cys171=)	rs1800389

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