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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126805765, NEXN
(E124K +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 20
+3 more
GUncertain significance
NEXN
(E267* +1 more)
Single nucleotide variant
(nonsense)
Dilated cardiomyopathy 1CC
+2 more
GConflicting classifications of pathogenicity
NEXN
(I483N +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 20
+1 more
GUncertain significance
NEXN
(G580E +1 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1CC
+2 more
GUncertain significance
NEXN
(Y652C +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
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