"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "WRN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 655112	NM_000553.6(WRN):c.497A>G (p.Asn166Ser)	WRN (N166S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 458490	NM_000553.6(WRN):c.586C>T (p.Arg196Cys)	WRN (R196C)	Single nucleotide variant (missense variant)	Werner syndrome +1 more	GUncertain significance
Select item 566883	NM_000553.6(WRN):c.1114_1115delinsC (p.Asp372fs)	WRN (D372fs)	Indel (frameshift variant)	Werner syndrome +1 more	GPathogenic/Likely pathogenic
Select item 2139816	NM_000553.6(WRN):c.1466C>A (p.Pro489Gln)	WRN (P489Q)	Single nucleotide variant (missense variant)	Werner syndrome +1 more	GUncertain significance
Select item 852444	NM_000553.6(WRN):c.3334T>C (p.Tyr1112His)	WRN (Y1112H)	Single nucleotide variant (missense variant)	Werner syndrome +1 more	GUncertain significance
Select item 135436	NM_000553.6(WRN):c.3785C>G (p.Thr1262Arg)	WRN (T1262R)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 135437	NM_000553.6(WRN):c.3875C>A (p.Ser1292Tyr)	WRN (S1292Y)	Single nucleotide variant (missense variant)	Werner syndrome +1 more	GConflicting classifications of pathogenicity
Select item 528131	NM_000553.6(WRN):c.3973G>A (p.Val1325Ile)	WRN (V1325I)	Single nucleotide variant (missense variant)	Werner syndrome +1 more	GUncertain significance

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