Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34210653
ALOX15
0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 8
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs4150407
ERCC3
1.000 0.120 2 127292055 3 prime UTR variant T/C snv 0.47 3
rs7817
IFRD1
0.925 0.200 7 112475603 3 prime UTR variant C/G;T snv 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3