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

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.1578del (p.Leu528fs)	rs780555196	0.00002
NM_000553.6(WRN):c.1114_1115delinsC (p.Asp372fs)	rs1563338855
NM_000553.6(WRN):c.1165del (p.Arg389fs)	rs878854131
NM_000553.6(WRN):c.1612_1615dup (p.Cys539fs)
NM_000553.6(WRN):c.2416del (p.Ile806fs)	rs1801528197
NM_000553.6(WRN):c.2826-1G>C	rs756880457
NM_000553.6(WRN):c.2968-1G>A	rs1300106191
NM_000553.6(WRN):c.348del (p.Met117fs)	rs1563329555

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