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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB6
(Q792* +1 more)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
ABCB6
(W776L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
ABCB6
(R739H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(R693C +1 more)
Single nucleotide variant
(missense variant)
ABCB6-related disorder
+2 more
GUncertain significance
ABCB6
(R723Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ABCB6
(R688H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ABCB6
(A635T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(A614V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(A614D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(R602Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
ABCB6
(A422S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(V408A +1 more)
Single nucleotide variant
(missense variant)
Microphthalmia, isolated, with coloboma 7
+4 more
GConflicting classifications of pathogenicity
ABCB6
(R230P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ABCB6
(C222F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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