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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNGA3
(R223W +1 more)
Single nucleotide variant
(missense variant)
Achromatopsia
+3 more
GPathogenic
CNGA3
(R277C +1 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
CNGA3
(H345R +1 more)
Single nucleotide variant
(missense variant)
Achromatopsia 2
+1 more
GConflicting classifications of pathogenicity
CNGA3
(V521M +1 more)
Single nucleotide variant
(missense variant)
Achromatopsia 2
+1 more
GUncertain significance
CNGA3
(T565M +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
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