Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3832566 | 8 | 105561297 | intron variant | A/- | delins | 0.29 | 1 | ||||
rs57942103 | 1.000 | 0.040 | 8 | 105501233 | intron variant | A/C | snv | 0.25 | 3 | ||
rs4734879 | 8 | 105570896 | intron variant | A/G | snv | 0.31 | 2 | ||||
rs284489 | 0.882 | 0.080 | 8 | 104945792 | intron variant | A/G | snv | 0.45 | 1 | ||
rs2343592 | 8 | 105560042 | intron variant | A/G | snv | 0.30 | 1 | ||||
rs16872085 | 8 | 104945312 | intron variant | A/G | snv | 7.6E-02 | 1 | ||||
rs4602861 | 8 | 105578478 | intron variant | A/G;T | snv | 1 | |||||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 7 | ||
rs7837523 | 8 | 105517074 | intron variant | A/T | snv | 0.80 | 1 | ||||
rs12546444 | 1.000 | 0.080 | 8 | 105346392 | intron variant | A/T | snv | 8.0E-02 | 1 | ||
rs4541868 | 8 | 105578477 | intron variant | C/A | snv | 0.33 | 1 | ||||
rs12678719 | 1.000 | 8 | 105503826 | intron variant | C/G | snv | 0.37 | 1 | |||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs2342781 | 1.000 | 0.040 | 8 | 105253492 | intron variant | C/G;T | snv | 1 | |||
rs284491 | 0.925 | 0.040 | 8 | 104946405 | intron variant | C/T | snv | 0.45 | 1 | ||
rs17210179 | 8 | 105333241 | intron variant | C/T | snv | 0.11 | 1 | ||||
rs72679151 | 8 | 104614889 | intron variant | C/T | snv | 0.17 | 1 | ||||
rs35783704 | 8 | 104954030 | intron variant | G/A | snv | 7.2E-02 | 2 | ||||
rs1350723 | 8 | 105218944 | intron variant | G/A | snv | 0.69 | 1 | ||||
rs1383592 | 8 | 105418448 | intron variant | G/A | snv | 0.26 | 1 | ||||
rs28416651 | 1.000 | 0.040 | 8 | 105552424 | intron variant | G/A;C | snv | 1 | |||
rs10093110 | 1.000 | 0.040 | 8 | 105553186 | intron variant | G/A;T | snv | 1 | |||
rs11774829 | 8 | 104966140 | intron variant | T/A | snv | 7.6E-02 | 3 | ||||
rs7819593 | 8 | 105102944 | intron variant | T/C | snv | 0.35 | 1 | ||||
rs7832219 | 8 | 105566749 | intron variant | T/C | snv | 0.31 | 1 |