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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRPH2
(G249S)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 7
GUncertain significance
PRPH2
(V209I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GLikely pathogenic
PRPH2
(D173A)
Single nucleotide variant
(missense variant)
PRPH2-Related Disorders
+1 more
GPathogenic/Likely pathogenic
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