Gene: MYH7 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727503269
rs727503269
MYH7
C 0.700 CausalMutation CLINVAR

dbSNP: rs727503272
rs727503272
MYH7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs727504236
rs727504236
MYH7
C 0.700 CausalMutation CLINVAR

dbSNP: rs727504272
rs727504272
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs727504280
rs727504280
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727505026
rs727505026
MYH7 ; MIR208B
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727505132
rs727505132
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880158
rs730880158
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880159
rs730880159
MYH7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs730880756
rs730880756
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880850
rs730880850
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs730880872
rs730880872
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs730880930
rs730880930
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs753392652
rs753392652
MYH7 ; MHRT
T 0.700 CausalMutation CLINVAR

dbSNP: rs863224900
rs863224900
MYH7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs876657887
rs876657887
MYH7
A 0.700 CausalMutation CLINVAR

dbSNP: rs878853842
rs878853842
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs886039185
rs886039185
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121913630
rs121913630
MYH7
A 0.740 CausalMutation CLINVAR Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. 1430197

1992
dbSNP: rs121913628
rs121913628
MYH7
T 0.700 CausalMutation CLINVAR Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations. 1430197

1992
dbSNP: rs121913627
rs121913627
MYH7
T 0.730 CausalMutation CLINVAR Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. 1552912

1992
dbSNP: rs121913625
rs121913625
MYH7
A 0.720 CausalMutation CLINVAR Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. 1552912

1992
dbSNP: rs121913626
rs121913626
MYH7
G 0.700 CausalMutation CLINVAR Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. 1552912

1992
dbSNP: rs3218713
rs3218713
MYH7
T 0.700 CausalMutation CLINVAR Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. 1552912

1992
dbSNP: rs121913624
rs121913624
MYH7
T 0.740 CausalMutation CLINVAR Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation. 1638703

1992