Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs2251219 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs33388 0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs17173608 0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs2391191 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs766288 0.790 0.080 1 231557942 intron variant G/T snv 0.40 7