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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA4, LOC126859766
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
LAMA4, LOC126859766
(S914Y +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
LAMA4, LOC126859766
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
LAMA4, LOC126859766
(V900I +1 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1JJ
+3 more
GConflicting classifications of pathogenicity
LOC126859766, LAMA4
(G896V +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+1 more
GUncertain significance
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