Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4360494 | 0.776 | 0.080 | 1 | 37990219 | upstream gene variant | G/C | snv | 0.45 | 12 | ||
rs6691170 | 0.776 | 0.080 | 1 | 221872104 | intergenic variant | G/T | snv | 0.34 | 12 | ||
rs61776719 | 0.776 | 0.120 | 1 | 37995647 | downstream gene variant | C/A | snv | 0.46 | 11 | ||
rs6687758 | 0.763 | 0.200 | 1 | 221991606 | regulatory region variant | A/G | snv | 0.20 | 11 | ||
rs12144319 | 0.776 | 0.080 | 1 | 54780362 | 3 prime UTR variant | T/C | snv | 0.31 | 10 | ||
rs1476413 | 0.790 | 0.360 | 1 | 11792243 | intron variant | C/G;T | snv | 4.0E-06; 0.26 | 0.23 | 10 | |
rs17011141 | 0.776 | 0.080 | 1 | 221939292 | intron variant | A/G | snv | 0.21 | 10 | ||
rs2297595 | 0.776 | 0.320 | 1 | 97699535 | missense variant | T/C | snv | 8.5E-02 | 8.1E-02 | 10 | |
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 10 | ||
rs369410616 | 0.752 | 0.280 | 1 | 45329400 | missense variant | C/T | snv | 2.0E-05 | 2.8E-05 | 10 | |
rs4846048 | 0.752 | 0.280 | 1 | 11786195 | 3 prime UTR variant | G/A | snv | 0.67 | 10 | ||
rs6678517 | 0.776 | 0.080 | 1 | 183033504 | intron variant | A/G;T | snv | 10 | |||
rs10911251 | 0.790 | 0.080 | 1 | 183112059 | intron variant | A/C | snv | 0.37 | 9 | ||
rs12143541 | 0.790 | 0.080 | 1 | 54782179 | intron variant | A/G | snv | 0.11 | 9 | ||
rs201395236 | 0.790 | 0.080 | 1 | 245018119 | intron variant | T/C | snv | 1.5E-04 | 9 | ||
rs2184857 | 0.790 | 0.080 | 1 | 239918447 | upstream gene variant | A/C | snv | 0.45 | 9 | ||
rs3753366 | 0.790 | 0.080 | 1 | 67729450 | intron variant | C/G | snv | 0.20 | 9 | ||
rs4546885 | 0.790 | 0.080 | 1 | 183056420 | intron variant | G/A;C | snv | 9 | |||
rs5277 | 0.790 | 0.160 | 1 | 186679065 | synonymous variant | C/G;T | snv | 0.12; 8.0E-06 | 9 | ||
rs658191 | 0.790 | 0.080 | 1 | 39458103 | non coding transcript exon variant | C/G | snv | 6.1E-02 | 9 | ||
rs6658977 | 0.790 | 0.080 | 1 | 221876478 | downstream gene variant | G/T | snv | 0.29 | 9 | ||
rs6691195 | 0.790 | 0.080 | 1 | 221989031 | downstream gene variant | C/A | snv | 0.19 | 9 | ||
rs72647484 | 0.790 | 0.080 | 1 | 22261235 | regulatory region variant | T/C | snv | 6.2E-02 | 9 | ||
rs7528276 | 0.790 | 0.080 | 1 | 39344315 | intron variant | T/A;C | snv | 9 | |||
rs7539542 | 0.807 | 0.200 | 1 | 202940846 | 3 prime UTR variant | G/C | snv | 0.58 | 9 |