Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14