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
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2251219 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs2498804 0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs187269 0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs3803300 0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs61749465 0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5