Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11