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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP418, CFAP418-AS1
+1 more
Single nucleotide variant
(synonymous variant)
Retinitis pigmentosa
+3 more
GConflicting classifications of pathogenicity
CFAP418, CFAP418-AS1
+1 more
(P19A)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GBenign/Likely benign