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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC2A10
(D39N)
Single nucleotide variant
(missense variant)
Arterial tortuosity syndrome
+2 more
GUncertain significance
SLC2A10
(V108I)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+3 more
GUncertain significance
SLC2A10
Single nucleotide variant
(synonymous variant)
Arterial tortuosity syndrome
+3 more
GBenign/Likely benign
SLC2A10
(R132W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SLC2A10
(Y216*)
Single nucleotide variant
(nonsense)
Arterial tortuosity syndrome
+1 more
GPathogenic/Likely pathogenic
SLC2A10
(A224G)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
SLC2A10
(A308V)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
SLC2A10
Single nucleotide variant
(synonymous variant)
Arterial tortuosity syndrome
+2 more
GLikely benign
SLC2A10
(A486T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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