C0043119[trait identifier] AND "GeneReviews"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 5449	NM_000553.6(WRN):c.1105C>T (p.Arg369Ter)	WRN (R369*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 38886	NM_000553.6(WRN):c.2089-3024A>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GPathogenic
Select item 38887	NM_000553.6(WRN):c.2179dup (p.Cys727fs)	WRN (C727fs)	Duplication (frameshift variant)	Werner syndrome	Gnot provided
Select item 38888	NM_000553.6(WRN):c.2500C>T (p.Arg834Cys)	WRN (R834C)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 5447	NM_000553.6(WRN):c.3139-1G>C	WRN	Single nucleotide variant (splice acceptor variant)	Werner syndrome	GPathogenic
Select item 38889	NM_000553.6(WRN):c.3460-2A>C	WRN	Single nucleotide variant (splice acceptor variant)	Werner syndrome	Gnot provided
Select item 38890	NM_000553.6(WRN):c.3590del (p.Asn1197fs)	WRN (N1197fs)	Deletion (frameshift variant)	Werner syndrome	GPathogenic/Likely pathogenic

ClinVar