Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
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
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs13001243 0.882 0.040 2 234306004 regulatory region variant G/A snv 7.5E-02 3
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3
rs201048567 0.882 0.040 7 125615031 intergenic variant CA/- delins 1.0E-05 3
rs2997119 0.882 0.040 13 55819766 intergenic variant A/G snv 0.52 3
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs56196471 0.882 0.040 4 178642661 intergenic variant G/A snv 2.9E-02 3
rs62482377 0.882 0.040 7 156250946 intergenic variant G/C snv 0.10 3