Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 5
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs4711268 1.000 6 31386727 upstream gene variant C/T snv 0.31 5
rs4711269 1.000 6 31387042 upstream gene variant C/T snv 0.32 5
rs7751505 1.000 6 31392478 downstream gene variant A/C snv 0.31 5
rs7751725 1.000 6 31392656 downstream gene variant A/G snv 0.31 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs3177928
HLA-DRA
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4
rs2305479
GSDMB
0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4