List of variants in gene WRN reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.513C>T (p.Cys171=)	rs1800389	0.66802
NM_000553.6(WRN):c.3222G>T (p.Leu1074Phe)	rs1801195	0.46398
NM_000553.6(WRN):c.3138+7G>A	rs2737335	0.46283
NM_000553.6(WRN):c.2361G>T (p.Leu787=)	rs1800392	0.44630
NM_000553.6(WRN):c.3138+6C>T	rs3024239	0.39769
NM_000553.6(WRN):c.4099T>C (p.Cys1367Arg)	rs1346044	0.22492

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