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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
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
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1445081098 0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17