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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFAP418
(K174R +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
CFAP418
(I171R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CFAP418, CFAP418-AS1
+1 more
Single nucleotide variant
(synonymous variant)
Retinitis pigmentosa
+3 more
GConflicting classifications of pathogenicity
CFAP418, LOC130000784
+1 more
(P19A)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign/Likely benign
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