Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7