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Links from MedGen

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNG2
(A174T +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GUncertain significance
CACNG2
(R296P +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GUncertain significance
CACNG2
(S23R +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GUncertain significance
CACNG2
(I200M +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GUncertain significance
CACNG2
(T292R +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GUncertain significance
CACNG2
(A100S +1 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
+1 more
GUncertain significance
CACNG2
(V120L)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 10
GPathogenic
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