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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126805765, NEXN
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 20
+3 more
GUncertain significance
LOC126805765, NEXN
(R113G +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
LOC126805765, NEXN
(Q50fs +1 more)
Deletion
(frameshift variant)
not provided
+2 more
GUncertain significance
LOC126805765, NEXN
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+5 more
GBenign
LOC126805765, NEXN
(R125* +1 more)
Single nucleotide variant
(nonsense)
Cardiomyopathy
GUncertain significance
LOC126805765, NEXN
(R127H +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
LOC126805765, NEXN
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 20
+2 more
GLikely benign
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