Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs7164773
RORA
0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 9
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7