Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
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
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
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
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 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
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 4
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 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
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
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3