Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs16982520
ZNF831
1.000 0.040 20 59183665 intron variant A/G snv 0.14 4
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs180070
LINC01497
0.882 0.040 17 69960745 upstream gene variant G/T snv 0.77 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs2820037 1.000 0.040 1 239273242 intergenic variant A/T snv 0.21 2
rs3739998
JCAD
1.000 0.040 10 30027143 missense variant C/A;G snv 4.0E-06; 0.38 3
rs4758685
MLXIP
1.000 0.040 12 122142295 3 prime UTR variant G/A snv 0.52 0.49 2
rs553350297
AGTR1
0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05 4
rs7136259
ATP2B1
1.000 0.040 12 89687411 intron variant T/A;C;G snv 2
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4
rs762079672
AGT
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06 4
rs7801190
SLC12A9
1.000 0.040 7 100860471 non coding transcript exon variant C/G snv 9.9E-02 2
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs1873077
CNTN3
0.925 0.080 3 74273636 intron variant T/C snv 0.24 4
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs4665630
KLHL29
0.925 0.080 2 23675447 intron variant C/T snv 0.78 3
rs7195830
CYBA
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7