List of variants studied for Werner syndrome by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000553.6(WRN):c.3422C>T (p.Ser1141Leu)	rs139323683	0.00052
NM_000553.6(WRN):c.229G>C (p.Asp77His)	rs144670883	0.00025
NM_000553.6(WRN):c.2114C>T (p.Thr705Ile)	rs141563618	0.00018
NM_000553.6(WRN):c.514A>C (p.Thr172Pro)	rs367991517	0.00010
NM_000553.6(WRN):c.2165A>G (p.Asn722Ser)	rs186693124	0.00005
NM_000553.6(WRN):c.2342C>T (p.Thr781Ile)	rs17847568	0.00003
NM_000553.6(WRN):c.192C>G (p.Phe64Leu)	rs1374804871	0.00001
NM_000553.6(WRN):c.610C>T (p.Pro204Ser)	rs199644081	0.00001
NM_000553.6(WRN):c.968C>T (p.Ser323Leu)	rs369277330	0.00001
NM_000553.6(WRN):c.15del (p.Lys5fs)	rs878854133
NM_000553.6(WRN):c.2089-3024A>G	rs281865157

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