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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPN1MW2
(A98T)
Single nucleotide variant
(missense variant)
Deuteranomaly
GUncertain significance
OPN1MW
(N94K)
Single nucleotide variant
(missense variant)
Deuteranomaly
GPathogenic
OPN1MW
Single nucleotide variant
Deuteranomaly
GPathogenic
OPN1MW
(R330Q)
Single nucleotide variant
(missense variant)
Deuteranomaly
GPathogenic
OPN1MW
(C203R)
Single nucleotide variant
(missense variant)
Cone monochromatism
+1 more
GPathogenic
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