Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 7
rs78478128
G6PD
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04 6
rs200111236
G6PD
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06 5
rs5030868
G6PD
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04 5
rs1050829
G6PD
0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02 3
rs5030872
G6PD
0.882 0.160 X 154534440 missense variant T/A snv 1.4E-04 4.7E-04 2
rs2071429
G6PD
0.925 0.160 X 154532293 intron variant G/A snv 0.63 2
rs2230037
G6PD
0.925 0.160 X 154532439 synonymous variant A/G snv 2
rs1050757
G6PD
0.925 0.160 X 154531643 3 prime UTR variant C/T snv 0.63 2
rs137852314
G6PD
0.851 0.120 X 154534495 missense variant C/T snv 4.4E-05 5.7E-05 2
rs137852335
G6PD
0.925 0.120 X 154532674 missense variant C/G snv 1
rs137852334
G6PD
0.925 0.120 X 154532695 missense variant G/A snv 1
rs387906470
G6PD
1.000 0.080 X 154532785 missense variant G/A snv 1
rs370451233
G6PD
1.000 0.040 X 154535315 missense variant T/C snv 1.1E-05 1.9E-05 1
rs137852320
G6PD
0.925 0.120 X 154532698 missense variant T/C snv 1
rs137852316
G6PD
0.925 0.120 X 154532676 missense variant C/T snv 1
rs72554664
G6PD
0.882 0.160 X 154532257 missense variant C/T snv 5.5E-04 1.1E-04 1
rs979416826
G6PD
1.000 0.040 X 154535247 missense variant G/A snv 1
rs76723693
G6PD
0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03 1
rs137852327
G6PD
0.882 0.120 X 154533122 missense variant C/T snv 2.2E-04 9.4E-05 1
rs370918918
G6PD
1.000 0.120 X 154535176 missense variant C/G snv 9.7E-04 8.5E-05 1
rs398123546
G6PD
0.925 0.120 X 154532390 missense variant G/A snv 1.5E-04 1.5E-04 1
rs145247580
G6PD
1.000 0.120 X 154534400 missense variant G/C snv 4.7E-04 6.2E-04 1
rs1193184183
IKBKG ; G6PD
1.000 0.080 X 154546076 missense variant T/C snv 1.9E-05 1