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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs137853011 0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 16
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 11
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs80358981 0.827 0.200 13 32356550 stop gained C/T snv 2.0E-05 1.4E-05 7
rs904571820 0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 5