"3billion"[submitter] AND "WRN"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 528108	NM_000553.6(WRN):c.835C>T (p.Arg279Trp)	WRN (R279W)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 404001	NM_000553.6(WRN):c.3893G>T (p.Gly1298Val)	WRN (G1298V)	Single nucleotide variant (missense variant)	Ovarian cancer +1 more	GConflicting classifications of pathogenicity