Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 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
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 6
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 6
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6