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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAR
(L1003P +5 more)
Single nucleotide variant
(missense variant)
Symmetrical dyschromatosis of extremities
GLikely pathogenic
ADAR, LOC126805874
(H589R +5 more)
Single nucleotide variant
(missense variant)
Symmetrical dyschromatosis of extremities
GLikely pathogenic
ADAR
(P213fs +1 more)
Deletion
(5 prime UTR variant +1 more)
Symmetrical dyschromatosis of extremities
GPathogenic
ADAR
(P193A +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
ADAR-related condition
+6 more
GConflicting classifications of pathogenicity
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