Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs3212948
ERCC1
0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 9
rs430397
HSPA5
0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs17849071
PIK3CA
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02 8
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs16893344
CCN4
0.807 0.160 8 133194036 intron variant C/T snv 0.29 7
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs2735971
MRPL23 ; H19
0.790 0.240 11 2000419 intron variant T/C snv 7
rs3212961
ERCC1
0.827 0.200 19 45419065 intron variant G/A;T snv 1.9E-04; 0.20 7
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7