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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYGB, PRCD
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
CYGB, PRCD
Single nucleotide variant
(splice donor variant)
Retinitis pigmentosa 36
GPathogenic
CYGB, PRCD
(M1T)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
+1 more
GPathogenic/Likely pathogenic
CYGB, PRCD
(R22*)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+1 more
GPathogenic
CYGB, PRCD
(C2Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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