Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 43 | ||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 12 | ||
rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
rs34720381 | 1 | 171486183 | intron variant | C/T | snv | 7.3E-02 | 4 | ||||
rs6809651 | 3 | 186096853 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs10513801 | 3 | 186104564 | intron variant | T/G | snv | 9.2E-02 | 3 | ||||
rs6968554 | 7 | 17247482 | 5 prime UTR variant | A/G;T | snv | 2 | |||||
rs6973656 | 7 | 77793266 | downstream gene variant | A/G;T | snv | 2 | |||||
rs72817412 | 16 | 89075082 | intergenic variant | C/A;T | snv | 2 |