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
rs9368649 0.925 0.040 6 30971106 intergenic variant A/G snv 0.10 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
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs148696809 0.851 0.160 6 28966575 downstream gene variant T/C snv 5.3E-02 4
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
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3