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
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs3758987 0.925 0.080 11 113904553 upstream gene variant T/C snv 0.32 4