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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT140, LOC105371046
(Q416*)
Single nucleotide variant
(nonsense)
Retinitis pigmentosa 80
GPathogenic
IFT140, LOC105371046
(P71L)
Single nucleotide variant
(missense variant)
Saldino-Mainzer syndrome
+3 more
GConflicting classifications of pathogenicity