List of variants reported as pathogenic for Werner syndrome by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.1105C>T (p.Arg369Ter)	rs17847577	0.00033
NM_000553.6(WRN):c.1165del (p.Arg389fs)	rs878854131
NM_000553.6(WRN):c.3244_3245del (p.Val1082fs)	rs770947623
NM_000553.6(WRN):c.3688-2A>G	rs2130469632

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