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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GJC2
(V66F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GJC2
(Y68C)
Single nucleotide variant
(missense variant)
Hypomyelinating leukodystrophy 2
+2 more
GPathogenic/Likely pathogenic
GJC2
(G186C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
GJC2
(P192R)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
GJC2
(Q248*)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
GJC2
(V258E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GJC2
(A322E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GJC2
(S392F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
GJC2
(T398I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
GJC2
(H412Y)
Single nucleotide variant
(missense variant)
Lymphatic malformation 3
+7 more
GUncertain significance
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