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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CERKL
Single nucleotide variant
(intron variant)
Severe photosensitivity
+3 more
GLikely pathogenic
TOPORS
(H889R +1 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 31
+8 more
GUncertain significance
C19orf12
(K142E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
C19orf12
(G69R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+8 more
GPathogenic/Likely pathogenic
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