Gene: MYH7 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501436
rs1060501436
MYH7
G 0.710 GeneticVariation CLINVAR

dbSNP: rs121913634
rs121913634
MYH7
A 0.710 CausalMutation CLINVAR

dbSNP: rs3218714
rs3218714
MYH7
C 0.710 GeneticVariation CLINVAR

dbSNP: rs397516260
rs397516260
MYH7
A 0.710 GeneticVariation CLINVAR

dbSNP: rs730880870
rs730880870
MYH7
A 0.710 GeneticVariation CLINVAR

dbSNP: rs1060501452
rs1060501452
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121913648
rs121913648
MYH7 ; MHRT
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913651
rs121913651
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs148808089
rs148808089
MYH7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555336492
rs1555336492
MYH7 ; MHRT
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1566531421
rs1566531421
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1566535410
rs1566535410
MYH7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1566536418
rs1566536418
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1566536436
rs1566536436
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs2069544
rs2069544
MYH7
C 0.700 CausalMutation CLINVAR

dbSNP: rs372381770
rs372381770
MYH7 ; MHRT
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397516115
rs397516115
MYH7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397516152
rs397516152
MYH7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516153
rs397516153
MYH7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516157
rs397516157
MYH7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs397516166
rs397516166
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397516246
rs397516246
MYH7 ; MHRT
T 0.700 GeneticVariation CLINVAR

dbSNP: rs606231324
rs606231324
MYH7
T 0.700 CausalMutation CLINVAR

dbSNP: rs727503261
rs727503261
MYH7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727503264
rs727503264
MYH7
G 0.700 GeneticVariation CLINVAR