Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
rs6700896 | 0.827 | 0.160 | 1 | 65624099 | intron variant | C/T | snv | 0.44 | 9 | ||
rs17342717 | 6 | 25821542 | intron variant | C/T | snv | 6.1E-02 | 8 | ||||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 7 | ||||
rs129128 | 6 | 26125114 | intron variant | C/T | snv | 0.91 | 7 | ||||
rs1505307 | 3 | 24301839 | intron variant | T/C | snv | 0.60 | 7 | ||||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 7 | ||
rs2283847 | 22 | 27785411 | intron variant | C/A;G;T | snv | 7 | |||||
rs7203560 | 1.000 | 0.080 | 16 | 134391 | intron variant | T/G | snv | 2.0E-02 | 7 | ||
rs737092 | 20 | 57415349 | regulatory region variant | T/C | snv | 0.58 | 7 | ||||
rs8176743 | 1.000 | 0.040 | 9 | 133256028 | missense variant | C/T | snv | 0.12 | 0.11 | 7 | |
rs8177318 | 3 | 133748533 | missense variant | T/A | snv | 1.6E-04 | 2.9E-04 | 7 | |||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 7 | ||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 7 | |||||
rs130624 | 22 | 37042611 | regulatory region variant | G/T | snv | 0.47 | 6 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs144861591 | 6 | 26072764 | intergenic variant | C/T | snv | 3.8E-02 | 6 | ||||
rs218237 | 4 | 54528005 | intergenic variant | C/T | snv | 0.18 | 6 | ||||
rs228129 | 22 | 37032558 | upstream gene variant | A/G | snv | 0.48 | 6 | ||||
rs2413450 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 6 | ||||
rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
rs3887266 | 0.925 | 0.120 | 6 | 25843518 | intron variant | C/T | snv | 8.9E-02 | 6 | ||
rs592423 | 6 | 139519556 | intron variant | A/C | snv | 0.50 | 6 |