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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCL
(V189L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
VCL
(D333E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
VCL
(P347S)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+4 more
GUncertain significance
VCL
(P347L)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+3 more
GUncertain significance
VCL
(R433H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GUncertain significance
VCL
(R520Q)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+3 more
GUncertain significance
VCL
(K666N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
VCL
(R680H)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+1 more
GUncertain significance
VCL
(P796fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1W
+1 more
GUncertain significance
VCL
(P796A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1W
+1 more
GUncertain significance
VCL
(P844L)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+4 more
GUncertain significance
VCL
(A990V +1 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GUncertain significance
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