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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAX2
(R179G)
Single nucleotide variant
(missense variant)
Age related macular degeneration 6
+2 more
GUncertain significance
RAX2
(D178G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAX2
(A160T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RAX2
(A144V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RAX2
(A144S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RAX2
(G141E)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
RAX2
(P138L)
Single nucleotide variant
(missense variant)
Age related macular degeneration 6
+3 more
GUncertain significance
RAX2
(S115L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAX2
(P112L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RAX2
(A105V)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
RAX2
(S92L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAX2
(V71M)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
RAX2
(V54G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RAX2
(E47K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
RAX2
(A45V)
Single nucleotide variant
(missense variant)
Age related macular degeneration 6
+3 more
GUncertain significance
RAX2
(H40Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RAX2
(R28Q)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
RAX2
(G8R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAX2
(E7K)
Single nucleotide variant
(missense variant)
Cone-rod dystrophy 11
+3 more
GConflicting classifications of pathogenicity
RAX2
(P5L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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