Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs5030868
G6PD
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04 9
rs1555570110
MPDU1
0.827 0.240 17 7586766 missense variant A/C snv 9
rs78478128
G6PD
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04 7
rs1050829
G6PD
0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02 5
rs137852314
G6PD
0.851 0.120 X 154534495 missense variant C/T snv 4.4E-05 5.7E-05 4
rs137852327
G6PD
0.882 0.120 X 154533122 missense variant C/T snv 2.2E-04 9.4E-05 3
rs5030872
G6PD
0.882 0.160 X 154534440 missense variant T/A snv 1.4E-04 4.7E-04 3
rs76723693
G6PD
0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03 3
rs1050757
G6PD
0.925 0.160 X 154531643 3 prime UTR variant C/T snv 0.63 2
rs137852328
G6PD
0.925 0.120 X 154534125 missense variant C/A;T snv 5.5E-06; 4.9E-05 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
rs398123546
G6PD
0.925 0.120 X 154532390 missense variant G/A snv 1.5E-04 1.5E-04 2
rs1281390228
DECR1
1.000 0.120 8 90036907 missense variant C/G snv 1
rs145247580
G6PD
1.000 0.120 X 154534400 missense variant G/C snv 4.7E-04 6.2E-04 1
rs2515904
G6PD
1.000 0.120 X 154534556 intron variant G/C snv 4.6E-02 1
rs370918918
G6PD
1.000 0.120 X 154535176 missense variant C/G snv 9.7E-04 8.5E-05 1