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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRIT3
(S175N)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1F
+3 more
GBenign
LRIT3
(M336L)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1F
+3 more
GBenign