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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPR143
(M121I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
GPR143
(Q25*)
Single nucleotide variant
(nonsense)
Ocular albinism, type I
+1 more
GPathogenic