Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6708166 | 2 | 30303914 | intron variant | G/A | snv | 0.32 | 2 | ||||
rs1869365 | 17 | 42141847 | intron variant | T/C | snv | 0.40 | 2 | ||||
rs4276643 | 8 | 27946082 | intron variant | C/T | snv | 0.64 | 2 | ||||
rs1070073 | 12 | 103606541 | intron variant | T/G | snv | 0.71 | 2 | ||||
rs4981022 | 12 | 103756096 | intron variant | G/A | snv | 0.69 | 2 | ||||
rs9390461 | 6 | 147380081 | intron variant | A/G | snv | 0.55 | 2 | ||||
rs4904820 | 14 | 91852591 | intron variant | G/A | snv | 0.53 | 2 | ||||
rs11064010 | 12 | 6050980 | intron variant | T/A;C | snv | 2 | |||||
rs2238109 | 12 | 6044801 | intron variant | T/A | snv | 0.40 | 2 | ||||
rs9271597 | 0.925 | 0.080 | 6 | 32623514 | upstream gene variant | T/A | snv | 0.39 | 3 | ||
rs9390460 | 6 | 147373198 | intron variant | T/C | snv | 0.51 | 3 | ||||
rs10102164 | 8 | 54509054 | upstream gene variant | G/A | snv | 0.19 | 4 | ||||
rs8176719 | 0.925 | 0.120 | 9 | 133257521 | frameshift variant | -/C | ins | 0.37 | 0.35 | 6 | |
rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 14 | ||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 18 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 |