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
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
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6