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Items: 37

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WRN
(K32R)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
(R36Q)
Single nucleotide variant
(missense variant)
WRN-related condition
+3 more
GConflicting classifications of pathogenicity
WRN
(D77H)
Single nucleotide variant
(missense variant)
Werner syndrome
+1 more
GUncertain significance
WRN
(V114I)
Single nucleotide variant
(missense variant)
Werner syndrome
+3 more
GBenign/Likely benign
WRN
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
WRN
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GPathogenic/Likely pathogenic
WRN
(N240K)
Single nucleotide variant
(missense variant)
WRN-related condition
+2 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
Werner syndrome
+1 more
GConflicting classifications of pathogenicity
WRN
(I257V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
WRN
(T324A)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
WRN
(E335D)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
WRN
(L383F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
WRN
(E510del)
Microsatellite
(inframe_deletion)
WRN-related condition
+2 more
GConflicting classifications of pathogenicity
WRN
(E510D)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
(V627I)
Single nucleotide variant
(missense variant)
Werner syndrome
+1 more
GConflicting classifications of pathogenicity
WRN
(R637W)
Single nucleotide variant
(missense variant)
WRN-related condition
+3 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
Werner syndrome
+2 more
GConflicting classifications of pathogenicity
WRN
(R834C)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
WRN
(A841T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
WRN
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
WRN
(L967fs)
Duplication
(frameshift variant)
not provided
GPathogenic
WRN
(L984I)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
WRN
(A995T)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
(D996N)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
(V1031L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
WRN
(R1033L)
Single nucleotide variant
(missense variant)
Werner syndrome
+1 more
GUncertain significance
WRN
Single nucleotide variant
(intron variant)
Werner syndrome
+1 more
GConflicting classifications of pathogenicity
WRN
(S1141L)
Single nucleotide variant
(missense variant)
WRN-related condition
+3 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
WRN
(T1262R)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
WRN
(S1292Y)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
WRN
Single nucleotide variant
(synonymous variant)
Werner syndrome
+1 more
GConflicting classifications of pathogenicity
WRN
(C1367R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
LOC126860342, WRN
(R1406*)
Single nucleotide variant
(nonsense)
not specified
+3 more
GConflicting classifications of pathogenicity
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