Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4958881 | 0.827 | 0.280 | 5 | 151070675 | intron variant | T/C | snv | 0.21 | 7 | ||
rs11864909 | 0.851 | 0.160 | 16 | 20389517 | intron variant | C/T | snv | 0.23 | 7 | ||
rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 7 | ||
rs4917014 | 0.807 | 0.360 | 7 | 50266267 | upstream gene variant | T/G | snv | 0.26 | 8 | ||
rs2275913 | 0.514 | 0.760 | 6 | 52186235 | upstream gene variant | G/A | snv | 0.28 | 105 | ||
rs3124954 | 1.000 | 0.080 | 9 | 134881650 | intron variant | C/T | snv | 0.32 | 1 | ||
rs12150220 | 0.724 | 0.360 | 17 | 5582047 | missense variant | A/T | snv | 0.37 | 0.33 | 14 | |
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 33 | |
rs2670660 | 0.708 | 0.400 | 17 | 5615686 | intron variant | A/G | snv | 0.41 | 15 | ||
rs7708392 | 0.732 | 0.400 | 5 | 151077924 | intron variant | G/C | snv | 0.44 | 13 | ||
rs6682654 | 0.882 | 0.320 | 1 | 160839213 | intron variant | G/A | snv | 0.45 | 3 | ||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs2004640 | 0.662 | 0.520 | 7 | 128938247 | splice donor variant | T/G | snv | 0.52 | 26 | ||
rs3766379 | 0.851 | 0.320 | 1 | 160837925 | intron variant | T/C | snv | 0.57 | 4 | ||
rs3758391 | 0.742 | 0.480 | 10 | 67883584 | upstream gene variant | T/C | snv | 0.64 | 11 |