Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 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
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
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
rs3751143 0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs3788266 0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs169068 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs956572 0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs6971 0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
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
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs694539 0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs734312 0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10