Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799777 | 9 | 104903754 | 5 prime UTR variant | -/C | delins | 0.10 | 1 | ||||
rs55951234 | 22 | 38205423 | 5 prime UTR variant | -/CTC | delins | 2 | |||||
rs111524356 | 2 | 65057022 | intron variant | -/GTGGATGCAGCAG;TGGATGCAGCAG;TGGATGCGGCAG;TGTATGCAGCAG | delins | 0.45 | 2 | ||||
rs142815467 | 19 | 46291277 | intergenic variant | -/T | delins | 0.12 | 3 | ||||
rs2980853 | 0.851 | 0.120 | 8 | 125466108 | upstream gene variant | A/C | snv | 0.43 | 16 | ||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 7 | ||||
rs4665710 | 2 | 20998163 | downstream gene variant | A/C | snv | 0.76 | 6 | ||||
rs11216126 | 1.000 | 0.040 | 11 | 116746524 | downstream gene variant | A/C | snv | 0.11 | 4 | ||
rs16991720 | 21 | 34484464 | intron variant | A/C | snv | 4 | |||||
rs2971672 | 7 | 44166307 | intron variant | A/C | snv | 0.44 | 4 | ||||
rs9972882 | 0.925 | 0.080 | 17 | 39651445 | intron variant | A/C | snv | 0.66 | 4 | ||
rs480392 | 1 | 107436774 | synonymous variant | A/C | snv | 0.99 | 0.95 | 3 | |||
rs6726798 | 2 | 218436132 | intron variant | A/C | snv | 0.94 | 3 | ||||
rs7000460 | 8 | 19946291 | intron variant | A/C | snv | 7.9E-02 | 3 | ||||
rs73059723 | 19 | 46293245 | upstream gene variant | A/C | snv | 0.12 | 3 | ||||
rs34515106 | 2 | 68380846 | missense variant | A/C | snv | 6.7E-03 | 1.9E-03 | 2 | |||
rs7519429 | 1 | 172380106 | intron variant | A/C | snv | 0.29 | 2 | ||||
rs10152811 | 15 | 86311359 | intron variant | A/C | snv | 0.28 | 1 | ||||
rs10861661 | 12 | 106780868 | intron variant | A/C | snv | 0.23 | 1 | ||||
rs12158587 | 22 | 25623573 | intron variant | A/C | snv | 2.8E-02 | 1 | ||||
rs1351452 | 11 | 117072638 | intron variant | A/C | snv | 0.86 | 1 | ||||
rs17058802 | 4 | 172722489 | intron variant | A/C | snv | 0.15 | 1 | ||||
rs1884507 | 20 | 52395625 | intron variant | A/C | snv | 0.11 | 1 | ||||
rs2227368 | 19 | 16896136 | non coding transcript exon variant | A/C | snv | 6.6E-03 | 2.6E-02 | 1 |