Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41507953
EPHX2
0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6
rs2233417
NFKBIA
1.000 0.080 14 35402888 intron variant C/T snv 0.14 0.13 1
rs1050851
NFKBIA
1.000 0.080 14 35403720 synonymous variant G/A snv 0.17 0.15 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246