Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs71297631 | 15 | 56369974 | intron variant | -/A | ins | 2 | |||||
rs35113840 | 2 | 238193015 | intron variant | -/A;AA | delins | 2 | |||||
rs112329286 | 1.000 | 0.080 | 14 | 63773159 | intron variant | -/ATTT | delins | 0.24 | 4 | ||
rs555594022 | 20 | 36983292 | intergenic variant | -/C | ins | 2 | |||||
rs34595852 | 9 | 86263457 | upstream gene variant | -/CT | delins | 0.75 | 2 | ||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs112908525 | 7 | 80675962 | intron variant | -/GGGTTGAGA | delins | 0.38 | 3 | ||||
rs201184664 | 17 | 59873258 | intron variant | -/GT | delins | 2 | |||||
rs150803770 | 3 | 49432529 | upstream gene variant | -/GTTTATTT;TTTTATTT;TTTTATTTATTT;TTTTATTTATTTATTT;TTTTATTTATTTATTTATTT | delins | 2 | |||||
rs79237498 | 7 | 6397234 | intron variant | -/T;TT | delins | 2 | |||||
rs548223088 | 20 | 37035116 | intron variant | -/TA | ins | 2 | |||||
rs35995659 | 14 | 58287055 | intron variant | -/TT | ins | 0.82 | 2 | ||||
rs200980971 | 6 | 109261139 | intron variant | A/-;AA | delins | 2 | |||||
rs11244669 | 10 | 125844213 | intron variant | A/C | snv | 0.28 | 4 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 4 | ||||
rs34338164 | 2 | 68388414 | missense variant | A/C | snv | 8.0E-03 | 7.8E-03 | 4 | |||
rs4953318 | 2 | 46127912 | intron variant | A/C | snv | 0.43 | 4 | ||||
rs138665726 | 22 | 21563570 | intron variant | A/C | snv | 0.17 | 3 | ||||
rs17302154 | 2 | 196183605 | intergenic variant | A/C | snv | 9.8E-02 | 3 | ||||
rs3169166 | 15 | 78270761 | intron variant | A/C | snv | 0.42 | 3 | ||||
rs10516140 | 5 | 179813910 | intron variant | A/C | snv | 0.76 | 2 | ||||
rs10923398 | 1 | 117708553 | regulatory region variant | A/C | snv | 0.16 | 2 | ||||
rs10952780 | 7 | 148857243 | intron variant | A/C | snv | 0.46 | 2 | ||||
rs11103379 | 9 | 136205504 | upstream gene variant | A/C | snv | 0.48 | 2 | ||||
rs111929233 | 12 | 124893863 | intergenic variant | A/C | snv | 9.5E-02 | 2 |