Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs16875288 0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs10494251 0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs1541187 0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs672607 0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325 0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs946903 0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs12649507 0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs231779 0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13