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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPR179
(R1031K)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1E
GUncertain significance
GPR179
(R639Q)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1E
+1 more
GUncertain significance
GPR179
(Q50*)
Single nucleotide variant
(nonsense)
Congenital stationary night blindness 1E
GLikely pathogenic
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