Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 10 | |||
rs12454712 | 0.925 | 0.120 | 18 | 63178651 | intron variant | T/A;C | snv | 9 | |||
rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 9 | ||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 9 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs4766578 | 0.851 | 0.200 | 12 | 111466567 | intron variant | T/A | snv | 0.66 | 8 | ||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 7 | ||||
rs112875651 | 8 | 125494452 | intron variant | G/A | snv | 0.31 | 7 | ||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 7 | ||||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 7 | |||||
rs11048456 | 1.000 | 0.080 | 12 | 26310149 | intron variant | C/T | snv | 0.62 | 6 | ||
rs4737010 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 6 | ||||
rs592423 | 6 | 139519556 | intron variant | A/C | snv | 0.50 | 6 | ||||
rs7133378 | 12 | 123924955 | intron variant | G/A | snv | 0.38 | 6 | ||||
rs766432 | 0.925 | 0.080 | 2 | 60492835 | intron variant | C/A | snv | 0.80 | 6 | ||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs1175550 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs13008603 | 2 | 46128709 | intron variant | C/A | snv | 0.10 | 5 | ||||
rs2022003 | 1 | 158617176 | intron variant | A/T | snv | 0.28 | 5 | ||||
rs2857078 | 17 | 44252803 | intron variant | A/C | snv | 0.62 | 5 | ||||
rs4434553 | 1.000 | 0.040 | 7 | 100642568 | intron variant | A/G | snv | 0.40 | 5 | ||
rs7246865 | 19 | 17108295 | intron variant | G/A | snv | 0.36 | 5 | ||||
rs74035509 | 16 | 88500925 | intron variant | C/T | snv | 0.10 | 5 | ||||
rs10947997 | 6 | 41953503 | intron variant | G/T | snv | 0.13 | 4 |