Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3918242 | 0.602 | 0.680 | 20 | 46007337 | upstream gene variant | C/T | snv | 0.14 | 1 | ||
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 5 | |||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 5 | ||
rs202085145 | 1.000 | 0.080 | 12 | 56002720 | missense variant | G/T | snv | 1.0E-03 | 5.6E-04 | 6 | |
rs5882 | 0.649 | 0.400 | 16 | 56982180 | missense variant | G/A;C | snv | 0.62 | 3 | ||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 7 | |||
rs7528604 | 0.925 | 0.040 | 1 | 65941669 | intron variant | G/A | snv | 0.42 | 2 | ||
rs34516333 | 16 | 73114768 | intron variant | G/T | snv | 0.17 | 1 | ||||
rs2451828 | 5 | 7448683 | intron variant | C/T | snv | 2.7E-02 | 1 | ||||
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 4 | |
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 11 | |
rs1458103 | 11 | 81336231 | intron variant | A/C | snv | 0.25 | 1 | ||||
rs342422 | 5 | 84175168 | intron variant | G/A;C | snv | 1 | |||||
rs16916239 | 8 | 86631513 | intron variant | A/G | snv | 0.16 | 1 | ||||
rs356219 | 0.776 | 0.240 | 4 | 89716450 | intron variant | G/A | snv | 0.54 | 1 | ||
rs356200 | 0.882 | 0.160 | 4 | 89747463 | intron variant | T/C | snv | 0.44 | 1 | ||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 2 | |||
rs6855911 | 0.851 | 0.200 | 4 | 9934286 | intron variant | A/G | snv | 0.33 | 4 |