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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A2
(I27M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC26A2
(R58C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
SLC26A2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
SLC26A2
(Y600H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SLC26A2
(T666A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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