Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17324272 1.000 X 133003128 intergenic variant T/C snv 3.2E-03 4
rs12122100 1.000 1 147037378 intron variant T/C snv 0.76 4
rs9497975 1.000 6 148226666 regulatory region variant G/A snv 3.1E-02 4
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3
rs17291045 1.000 4 160585745 intron variant C/T snv 9.3E-02 4
rs38152 1.000 7 20007952 intron variant A/C snv 6.2E-02 4
rs12185555 1.000 2 226694601 regulatory region variant A/G snv 0.25 4
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs2741012 1.000 2 233600317 upstream gene variant C/T snv 0.24 1
rs10173355 1.000 2 233688675 intron variant A/G;T snv 1
rs17863787 0.925 0.040 2 233702448 intron variant T/G snv 0.30 3
rs1875263 1.000 2 233716976 intron variant C/G;T snv 3
rs4663969 1.000 2 233746667 intron variant C/A;T snv 2
rs3755319 0.925 0.120 2 233758936 intron variant A/C;G;T snv 3
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs4148325 0.851 0.080 2 233764663 intron variant C/T snv 0.36 3
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs7758512 1.000 6 30002812 intron variant T/G snv 0.17 4
rs9261129 1.000 6 30011802 intron variant T/C snv 0.17 4
rs9261174 1.000 6 30029078 intron variant T/C snv 0.17 4
rs3869068 0.925 6 30036275 intron variant C/T snv 0.17 4
rs259919 0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs2301753 0.925 0.040 6 30071463 missense variant G/T snv 0.18 0.17 4