Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs390802
DNAH1
0.827 0.160 3 52397655 intron variant G/A snv 0.16 5
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4
rs11894252
EPAS1
0.925 0.120 2 46306237 intron variant T/A;C;G snv 3
rs1609682
IL1A
0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs2243267
IL4
0.882 0.160 5 132678194 intron variant G/A;C snv 3
rs2243289
LOC105379176 ; IL4
0.882 0.240 5 132682440 intron variant A/G snv 0.26 0.23 3
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs10771279
ITPR2
0.925 0.120 12 26377610 intron variant T/A;C snv 0.40 2
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2
rs1259293
FSTL1
0.925 0.120 3 120421014 intron variant T/C snv 0.59 2
rs12617313
EPAS1
0.925 0.120 2 46332637 intron variant A/G;T snv 2
rs2243270
IL4
0.925 0.120 5 132678417 intron variant A/G;T snv 2
rs2291599
DKK3
0.925 0.120 11 11968352 intron variant T/C snv 0.83 0.85 2
rs2499707
GRM4
0.925 0.120 6 34085889 intron variant T/A;C snv 2
rs2504106
DAAM2
0.925 0.120 6 39854343 intron variant A/G snv 0.61 2
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs3923594
MCAM
1.000 0.120 11 119317205 intron variant C/A;T snv 7.1E-06 2
rs4381241
FAF1
0.925 0.120 1 50441766 intron variant T/C snv 0.51 2
rs4765623
SCARB1
0.925 0.120 12 124836304 intron variant C/T snv 0.38 2
rs4787951
IL4R
0.925 0.120 16 27332642 intron variant T/C snv 0.29 2
rs4903064
DPF3
0.925 0.120 14 72812712 intron variant T/C snv 0.23 2
rs6442260
ATG7
0.925 0.160 3 11549277 intron variant G/A snv 0.42 2
rs6641352
MAGEA11
0.925 0.120 X 149711150 intron variant A/G snv 2