Gene: MYH7 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913624
rs121913624
MYH7
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913625
rs121913625
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913626
rs121913626
MYH7
G 0.800 CausalMutation CLINVAR

dbSNP: rs121913626
rs121913626
MYH7
T 0.800 GeneticVariation CLINVAR

dbSNP: rs121913632
rs121913632
MYH7
G 0.800 CausalMutation CLINVAR

dbSNP: rs121913633
rs121913633
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913634
rs121913634
MYH7
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913636
rs121913636
MYH7
C 0.800 CausalMutation CLINVAR

dbSNP: rs121913638
rs121913638
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913639
rs121913639
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913650
rs121913650
MYH7 ; MHRT
A 0.800 CausalMutation CLINVAR

dbSNP: rs121913651
rs121913651
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs202141173
rs202141173
MYH7
T 0.800 GeneticVariation CLINVAR

dbSNP: rs202141173
rs202141173
MYH7
0.800 GeneticVariation UNIPROT

dbSNP: rs267606908
rs267606908
MYH7
C 0.800 CausalMutation CLINVAR

dbSNP: rs267606910
rs267606910
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs267606911
rs267606911
MYH7
A 0.800 CausalMutation CLINVAR

dbSNP: rs3218713
rs3218713
MYH7
A 0.800 GeneticVariation CLINVAR

dbSNP: rs3218716
rs3218716
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs376897125
rs376897125
MYH7
T 0.800 GeneticVariation CLINVAR

dbSNP: rs397516127
rs397516127
MYH7
A 0.800 CausalMutation CLINVAR

dbSNP: rs397516171
rs397516171
MYH7
G 0.800 GeneticVariation CLINVAR

dbSNP: rs397516209
rs397516209
MYH7
T 0.800 CausalMutation CLINVAR

dbSNP: rs727503246
rs727503246
MYH7 ; MIR208B
0.800 GeneticVariation UNIPROT

dbSNP: rs727503260
rs727503260
MYH7
0.800 GeneticVariation UNIPROT