Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1559931177 0.827 0.120 3 49047207 stop gained G/A snv 34
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15