Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4
rs7219923
GSDMB
0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs9303281
GSDMB
0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 3
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 3
rs176095
PBX2 ; GPSM3
0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs2523477 0.925 0.080 6 31392612 downstream gene variant T/C snv 0.10 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3