Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 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
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
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
rs12449964 1.000 0.040 17 17641390 regulatory region variant C/T snv 0.36 2
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
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
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5