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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPM1
(R624C +2 more)
Single nucleotide variant
(missense variant)
Congenital stationary night blindness 1C
GLikely pathogenic
TRPM1
Single nucleotide variant
(synonymous variant)
Congenital stationary night blindness 1C
+1 more
GConflicting classifications of pathogenicity