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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPM1
(R877* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
TRPM1
(W856* +2 more)
Single nucleotide variant
(nonsense)
TRPM1-related disorder
GPathogenic
TRPM1
Single nucleotide variant
(synonymous variant)
Congenital stationary night blindness 1C
+1 more
GConflicting classifications of pathogenicity
TRPM1
(K294* +2 more)
Single nucleotide variant
(nonsense)
Congenital stationary night blindness
GPathogenic
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