Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs2305479
GSDMB
0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs7219923
GSDMB
0.882 0.160 17 39918265 non coding transcript exon 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
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs7224129
GSDMB
0.925 0.160 17 39919173 non coding transcript exon variant G/A snv 0.52 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs9303280
GSDMB
1.000 0.080 17 39917778 non coding transcript exon variant T/A;C snv 2
rs11078928
GSDMB
0.925 0.160 17 39908216 splice acceptor variant T/A;C snv 0.40 1