Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 10 | ||||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 9 | |||
rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs1358980 | 6 | 43796814 | intergenic variant | C/T | snv | 0.40 | 6 | ||||
rs9930333 | 0.882 | 0.120 | 16 | 53766065 | intron variant | T/C;G | snv | 5 | |||
rs1936807 | 6 | 127127104 | intron variant | C/G | snv | 0.55 | 4 | ||||
rs571312 | 1.000 | 0.080 | 18 | 60172536 | intergenic variant | C/A | snv | 0.26 | 4 | ||
rs718314 | 0.882 | 0.120 | 12 | 26300350 | intron variant | A/G | snv | 0.27 | 4 | ||
rs4738141 | 8 | 71557507 | intron variant | A/G | snv | 0.41 | 3 |