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
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs11174202 0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs11783752 0.925 0.040 8 20192013 intergenic variant G/A;C snv 2
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs4825476 0.925 0.040 X 123307628 intron variant G/A;C snv 2
rs75063949 0.925 0.040 6 25590813 intron variant C/G snv 0.14 2