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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2044081 1.000 0.080 4 47216323 intron variant C/T snv 0.14 2