Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9