Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17249754 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 12 | ||
rs3774372 | 1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 | 4 | |
rs13139571 | 1.000 | 0.040 | 4 | 155724361 | intron variant | C/A | snv | 0.22 | 9 | ||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 10 | ||
rs381815 | 1.000 | 0.040 | 11 | 16880721 | intron variant | C/A;T | snv | 0.24 | 6 | ||
rs11014166 | 0.882 | 0.040 | 10 | 18419869 | intron variant | A/T | snv | 0.27 | 10 | ||
rs12940887 | 17 | 49325445 | intron variant | C/T | snv | 0.28 | 5 | ||||
rs1813353 | 10 | 18418519 | intron variant | T/C | snv | 0.29 | 5 | ||||
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs1573643 | 15 | 90877743 | intron variant | T/C | snv | 0.33 | 5 | ||||
rs932764 | 10 | 94136183 | intron variant | A/G | snv | 0.38 | 6 | ||||
rs35441 | 12 | 115115310 | intergenic variant | C/T | snv | 0.40 | 5 | ||||
rs805303 | 0.925 | 0.160 | 6 | 31648589 | intron variant | G/A | snv | 0.45 | 7 | ||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs1327235 | 20 | 10988382 | intron variant | A/G | snv | 0.46 | 7 | ||||
rs1731249 | 2 | 26697157 | intron variant | T/A | snv | 0.48 | 5 | ||||
rs7823056 | 8 | 8525195 | intergenic variant | A/G | snv | 0.55 | 3 | ||||
rs438885 | 2 | 164195781 | intron variant | A/T | snv | 0.56 | 5 | ||||
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 9 | ||||
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs5883070 | 7 | 27240226 | intron variant | -/AAAACA;AACA | delins | 0.91 | 5 |