U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 1 to 100 of 145

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYL2
Single nucleotide variant
(3 prime UTR variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 10
+3 more
GLikely benign
MYL2
(I159V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
MYL2
(I158V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
MYL2
(K153N)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+5 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
(L150S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
MYL2
(G148fs)
Insertion
(frameshift variant)
Cardiomyopathy
GUncertain significance
MYL2
(T147fs)
Duplication
(frameshift variant)
Cardiomyopathy
GUncertain significance
MYL2
(V146M)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 10
+3 more
GLikely benign
MYL2
(D145Y)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
(D145N)
Single nucleotide variant
(missense variant)
not specified
+6 more
GUncertain significance
MYL2
(P144fs)
Deletion
(frameshift variant)
Hypertrophic cardiomyopathy
+3 more
GConflicting classifications of pathogenicity
MYL2
(P144H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+1 more
GUncertain significance
MYL2
(P144S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MYL2
(P144A)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+3 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
(F142L)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
MYL2
(A141D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 10
+3 more
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+2 more
GLikely benign
MYL2
(M138K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+3 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 10
+1 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 10
+1 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 10
+1 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 10
+2 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
(E134A)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
MYL2
(S131T +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
MYL2
(Q126E)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GLikely benign
MYL2
(T125M)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
MYL2
(R120Q)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+5 more
GConflicting classifications of pathogenicity
MYL2
(R120G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+5 more
GUncertain significance
MYL2
(R120W)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GUncertain significance
MYL2
(V119I)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy
+2 more
GUncertain significance
MYL2
(A116V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+5 more
GBenign/Likely benign
MYL2
(L114R)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
(V99fs +2 more)
Duplication
(frameshift variant)
Cardiomyopathy
GUncertain significance
MYL2
(F106fs)
Deletion
(frameshift variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GLikely benign
MYL2
(K104Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
(K104E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
(L100fs)
Deletion
(frameshift variant)
Cardiovascular phenotype
+2 more
GUncertain significance
MYL2
(F103C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYL2
(A102S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
MYL2
(N101S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
(L100V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign/Likely benign
MYL2
Single nucleotide variant
(splice acceptor variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(splice acceptor variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 10
+3 more
GBenign/Likely benign
MYL2
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MYL2
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYL2
(F86S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
MYL2
(F86L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+4 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
MYL2
(V81M)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GLikely benign
MYL2
(P74L)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
MYL2
(E72D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
MYL2
(M69T)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+3 more
GUncertain significance
MYL2
(N63fs)
Deletion
(frameshift variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MYL2
(K62*)
Single nucleotide variant
(nonsense)
Hypertrophic cardiomyopathy 10
+3 more
GConflicting classifications of pathogenicity
MYL2
(V61M)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+3 more
GUncertain significance
MYL2
(V59E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy
+3 more
GLikely benign
MYL2
(G57E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant +1 more)
Cardiomyopathy
GLikely benign
MYL2
Microsatellite
(intron variant)
Hypertrophic cardiomyopathy 10
+2 more
GLikely benign
MYL2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+1 more
GLikely benign
MYL2
(A54V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 10
+3 more
GLikely benign
MYL2
(D51Y)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 10
+1 more
GLikely benign
MYL2
(D48E)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYL2
(D48H)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYL2
(D48N)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 10
+3 more
GUncertain significance
MYL2
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GLikely benign
MYL2
(N47K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+7 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination