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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NHS
(D182E)
Single nucleotide variant
(missense variant)
Cataract 40
+1 more
GUncertain significance
NHS
Single nucleotide variant
(synonymous variant)
Nance-Horan syndrome
GConflicting classifications of pathogenicity
NHS
(S1528P +3 more)
Single nucleotide variant
(missense variant)
Nance-Horan syndrome
GUncertain significance
NHS
(T1574P +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ACE2, ACOT9
+94 more
Copy number gain
not provided
GPathogenic
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