Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs784257
LOC105372130
1.000 0.080 18 55729968 intron variant T/A;C snv 4
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72 3
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs146311723
USP3
1.000 0.080 15 63512308 intron variant T/C snv 0.14 2
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 2
rs6535594
NR3C2
4 148211605 intron variant G/A snv 0.54 2
rs67339103
LRMDA
10 76133928 intron variant G/A;C;T snv 2
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs10207567
ICA1L
2 202850250 intron variant G/A;C snv 1
rs11162351
AK5
1 77479047 intron variant C/G snv 0.31 1
rs1124694
LINC02752
11 11077129 intron variant A/G;T snv 1
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs1145074
SPATA5L1
15 45411626 intron variant T/A;G snv 0.45 1
rs12032996 1 33454985 intergenic variant G/A snv 0.12 1
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1
rs12727980
LINC00862
1 200289967 intron variant C/T snv 0.54 1
rs1276720
CUBN
10 16929427 intron variant C/T snv 0.65 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs17368443
SBF2
11 10275289 intron variant G/C snv 5.3E-02 1