Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 10 | ||||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 9 | |||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 9 | |||
rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 9 | ||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 7 | |||||
rs863750 | 12 | 124020897 | intron variant | C/T | snv | 0.53 | 7 | ||||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs1358980 | 6 | 43796814 | intergenic variant | C/T | snv | 0.40 | 6 | ||||
rs1045241 | 1.000 | 0.120 | 5 | 119393591 | 3 prime UTR variant | C/T | snv | 0.30 | 5 | ||
rs9991328 | 4 | 88791970 | intron variant | C/T | snv | 0.53 | 5 |