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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRM6, ZNF454
(S685W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
GRM6
(V243F)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1B
+2 more
GBenign/Likely benign