Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs7577262 2 233910224 intergenic variant G/A;T snv 4
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs2980755 8 8506173 intergenic variant A/G snv 0.46 3
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs13178964 5 105011948 intron variant A/G snv 0.17 2
rs133980 22 27626764 intergenic variant A/G snv 0.42 2
rs4573996 18 78734592 intergenic variant G/A snv 0.12 2
rs576603 11 1892909 upstream gene variant C/A;G;T snv 2
rs9561252 13 93077032 intergenic variant A/G snv 7.2E-02 2
rs10850411 12 114949991 intergenic variant T/C snv 0.34 1