rs3782889, MYL2

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.800 1.000 1 2013 2013
Drinking behavior processes
CUI: C0013124
Disease: Drinking behavior processes
31 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.700 1.000 2 2011 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.700 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.010 1.000 1 2014 2014
Obesity
CUI: C0028754
Disease: Obesity
1111 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.010 1.000 1 2016 2016