Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10159239
NLRP3
0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
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
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10918859
NOS1AP
0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
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
rs12040273
GALNT2
0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs12050217
BDKRB1
0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs12115090
CRISPLD1
0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs12704673
CALCR
0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13306221
BDNF
0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15