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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRPH2
(D338G)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+10 more
GBenign
PRPH2
(W246R)
Single nucleotide variant
(missense variant)
Vitelliform macular dystrophy 3
GLikely pathogenic
PRPH2
(G167S)
Single nucleotide variant
(missense variant)
PRPH2-Related Disorders
+3 more
GPathogenic/Likely pathogenic
PRPH2
(G137D)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+1 more
GPathogenic/Likely pathogenic
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