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
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
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs6269 0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs1390938 0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs2268498 0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs301430 0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs1843809 0.851 0.080 12 71954918 intron variant G/T snv 0.77 6