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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHX38
(R324Q)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 84
GLikely pathogenic
DHX38
(G332D)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 84
GUncertain significance