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Items: 1 to 100 of 139

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH6
(E1916D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYH6
(K1881R)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(splice acceptor variant)
Cardiomyopathy
GBenign
MYH6
Single nucleotide variant
(intron variant)
Cardiomyopathy
GBenign
MYH6
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GLikely benign
MYH6
(G1826N)
Indel
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 1
+8 more
GBenign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+5 more
GBenign/Likely benign
MYH6
(Q1804K)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign/Likely benign
MYH6
(A1765T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GConflicting classifications of pathogenicity
LOC126861896, MYH6
(V1693M)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+7 more
GConflicting classifications of pathogenicity
LOC126861896, MYH6
(R1664H)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+4 more
GBenign/Likely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
LOC126861896, MYH6
Single nucleotide variant
(intron variant)
Atrial septal defect 3
+7 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 14
+4 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign/Likely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GBenign
LOC126861896, MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
LOC126861896, MYH6
(H1555Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GBenign/Likely benign
MYH6
(A1489T)
Single nucleotide variant
(missense variant)
MYH6-related disorder
+3 more
GUncertain significance
MYH6
Single nucleotide variant
(intron variant)
not specified
+7 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(intron variant)
Cardiomyopathy
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(intron variant)
not provided
+4 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
MYH6
(E1403K)
Single nucleotide variant
(missense variant)
MYH6-related disorder
+4 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+8 more
GBenign
MYH6
(R1398Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GLikely benign
MYH6
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GLikely benign
MYH6
(T1379M)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYH6
(R1346W)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
MYH6
Deletion
(intron variant)
Atrial septal defect 3
+5 more
GLikely benign
MYH6
Deletion
(intron variant)
not specified
+2 more
GConflicting classifications of pathogenicity
MYH6
Duplication
Hypertrophic cardiomyopathy 14
+3 more
GBenign/Likely benign
MYH6
Deletion
(intron variant)
Cardiomyopathy
+3 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign
MYH6
Duplication
(intron variant)
Dilated Cardiomyopathy, Dominant
+5 more
GConflicting classifications of pathogenicity
MYH6
Indel
(intron variant)
Hypertrophic cardiomyopathy 14
+3 more
GConflicting classifications of pathogenicity
MYH6
Deletion
(intron variant)
not specified
+5 more
GBenign/Likely benign
MYH6
Deletion
(intron variant)
Hypertrophic cardiomyopathy 14
+2 more
GBenign
MYH6
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1EE
+7 more
GBenign/Likely benign
MYH6
Deletion
(intron variant)
Hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 14
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 14
+3 more
GBenign
MYH6
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+8 more
GBenign/Likely benign
MYH6
(E1295Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GBenign/Likely benign
MYH6
(L1289F)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MYH6
(L1282V)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+2 more
GLikely benign
MYH6
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 14
+4 more
GBenign/Likely benign
MYH6
(T1190I)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
GLikely benign
MYH6
(E1170K)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GBenign
MYH6
(S1149R)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
MYH6
(R1143Q)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
MYH6
(A1130T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GBenign
MYH6
(R1128H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+10 more
GUncertain significance
MYH6
Deletion
(intron variant)
Hypertrophic cardiomyopathy 14
+4 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MYH6
(D1060N)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MYH6
(R1052*)
Single nucleotide variant
(nonsense)
Hypertrophic cardiomyopathy 14
+4 more
GUncertain significance
MYH6
(A1004S)
Single nucleotide variant
(missense variant)
not specified
+8 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+8 more
GBenign
MYH6
Single nucleotide variant
(intron variant)
Atrial septal defect 3
+6 more
GBenign/Likely benign
MYH6
(R943H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+2 more
GUncertain significance
MYH6
(A936T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+1 more
GUncertain significance
MYH6
(A936S)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+7 more
GLikely benign
MYH6
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 1
+6 more
GLikely benign
MYH6
(R872C)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
MYH6
(R871H)
Single nucleotide variant
(missense variant)
Atrial septal defect 3
+7 more
GUncertain significance
MYH6
(R871C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GUncertain significance
MYH6
(R860H)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
MYH6
(G859R)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
MYH6
(G859W)
Single nucleotide variant
(missense variant)
Sick sinus syndrome 3, susceptibility to
+8 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+1 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 14
+4 more
GBenign/Likely benign
MYH6
(R795W)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 14
+8 more
GUncertain significance
MYH6
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1EE
+7 more
GLikely benign
MYH6
(V691I)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+9 more
GBenign/Likely benign
MYH6
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GLikely benign
MYH6
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 14
+1 more
GConflicting classifications of pathogenicity
MYH6
(D588A)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
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