Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2410373 | 0.851 | 0.120 | 8 | 16066997 | intergenic variant | A/C | snv | 0.34 | 6 | ||
rs16917302 | 0.851 | 0.080 | 10 | 62501439 | intron variant | A/C | snv | 0.18 | 5 | ||
rs1870050 | 0.827 | 0.160 | 15 | 51344354 | intron variant | A/C | snv | 6.0E-02 | 5 | ||
rs190900046 | 0.827 | 0.160 | 17 | 43104197 | synonymous variant | A/C | snv | 8.0E-06 | 4.2E-05 | 5 | |
rs6180 | 0.827 | 0.160 | 5 | 42719137 | missense variant | A/C | snv | 0.44 | 0.43 | 5 | |
rs833052 | 0.827 | 0.160 | 6 | 43755598 | intergenic variant | A/C | snv | 0.88 | 5 | ||
rs11895168 | 0.925 | 0.080 | 2 | 211377467 | 3 prime UTR variant | A/C | snv | 0.68 | 4 | ||
rs2296135 | 0.851 | 0.080 | 10 | 5952731 | 3 prime UTR variant | A/C | snv | 0.58 | 4 | ||
rs3864659 | 0.925 | 0.080 | 8 | 140545763 | intron variant | A/C | snv | 0.16 | 4 | ||
rs4987208 | 0.851 | 0.160 | 12 | 913403 | stop gained | A/C | snv | 3.5E-02 | 2.1E-02 | 4 | |
rs7713645 | 0.851 | 0.200 | 5 | 68231498 | intron variant | A/C | snv | 0.58 | 4 | ||
rs8004379 | 0.851 | 0.120 | 14 | 33599495 | intron variant | A/C | snv | 0.12 | 4 | ||
rs981782 | 0.851 | 0.080 | 5 | 45285616 | intron variant | A/C | snv | 0.34 | 4 | ||
rs985325188 | 0.851 | 0.080 | 14 | 20456806 | missense variant | A/C | snv | 4 | |||
rs13423759 | 0.925 | 0.080 | 2 | 211381247 | 3 prime UTR variant | A/C | snv | 6.8E-02 | 3 | ||
rs15869 | 0.925 | 0.080 | 13 | 32398875 | 3 prime UTR variant | A/C | snv | 0.15 | 3 | ||
rs2071002 | 0.882 | 0.080 | 6 | 3000069 | 5 prime UTR variant | A/C | snv | 0.32 | 3 | ||
rs2787486 | 0.925 | 0.080 | 17 | 55132413 | intron variant | A/C | snv | 0.33 | 3 | ||
rs34434221 | 0.882 | 0.080 | 15 | 85579644 | missense variant | A/C | snv | 2.2E-02 | 2.2E-02 | 3 | |
rs406113 | 0.882 | 0.160 | 6 | 28515705 | missense variant | A/C | snv | 0.38 | 0.45 | 3 | |
rs7719521 | 0.882 | 0.120 | 5 | 151669843 | intron variant | A/C | snv | 0.65 | 3 | ||
rs10043985 | 0.925 | 0.080 | 5 | 111065770 | upstream gene variant | A/C | snv | 5.2E-02 | 2 | ||
rs11085735 | 0.925 | 0.080 | 19 | 10491504 | intron variant | A/C | snv | 0.92 | 2 | ||
rs12239582 | 0.925 | 0.080 | 1 | 76371552 | intron variant | A/C | snv | 0.30 | 2 | ||
rs1326306 | 0.925 | 0.080 | 13 | 31364049 | intergenic variant | A/C | snv | 0.67 | 2 |