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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRPH2
Single nucleotide variant
(3 prime UTR variant)
Vitelliform macular dystrophy 3
+8 more
GBenign
PRPH2
(D338G)
Single nucleotide variant
(missense variant)
Choroidal dystrophy, central areolar 2
+10 more
GBenign
PRPH2
(R310K)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 7
+11 more
GBenign
PRPH2
(Q304E)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 7
+10 more
GBenign
PRPH2
Single nucleotide variant
(synonymous variant)
Vitelliform macular dystrophy 3
+10 more
GBenign
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