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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT172
(A776V)
Single nucleotide variant
(missense variant)
Nephronophthisis
GUncertain significance
IFT172
(R432H)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 71
+2 more
GUncertain significance