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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNNM2
(G16E)
Single nucleotide variant
(missense variant)
Hypomagnesemia, seizures, and intellectual disability 1
+2 more
GUncertain significance
CNNM2
Deletion
(inframe_deletion)
not provided
GUncertain significance
CNNM2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CNNM2
(L334R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CNNM2
(L522F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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