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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ENPP1
(S162G)
Single nucleotide variant
(missense variant)
ENPP1-related disorder
+1 more
GUncertain significance
ENPP1
(R481W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
ENPP1
(Y551C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ENPP1
(H777R)
Single nucleotide variant
(missense variant)
not provided
+7 more
GUncertain significance
ARG1, AKAP7
+15 more
Copy number loss
not provided
GLikely pathogenic
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