Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9271366 | 0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 | 9 | ||
rs7194886 | 0.851 | 0.080 | 16 | 50691282 | upstream gene variant | C/T | snv | 0.38 | 4 | ||
rs2844573 | 0.882 | 0.160 | 6 | 31367677 | intron variant | A/C;G | snv | 3 | |||
rs4574921 | 0.882 | 0.160 | 9 | 114776054 | upstream gene variant | C/T | snv | 0.80 | 3 | ||
rs9271348 | 0.925 | 0.160 | 6 | 32615965 | regulatory region variant | G/A | snv | 0.74 | 2 | ||
rs9302752 | 0.925 | 0.120 | 16 | 50685192 | upstream gene variant | T/C | snv | 0.68 | 2 | ||
rs10982385 | 1.000 | 0.040 | 9 | 114730737 | intergenic variant | T/G | snv | 0.47 | 1 | ||
rs13220141 | 1.000 | 0.040 | 6 | 146576497 | intergenic variant | A/T | snv | 8.2E-02 | 1 | ||
rs1587601 | 1.000 | 0.040 | 5 | 35254508 | intergenic variant | A/G | snv | 0.64 | 1 | ||
rs160451 | 1.000 | 0.040 | 8 | 89650713 | intron variant | T/C | snv | 0.56 | 1 | ||
rs16948876 | 1.000 | 0.040 | 16 | 50820507 | intergenic variant | G/A | snv | 6.2E-02 | 1 | ||
rs28490179 | 1.000 | 0.040 | 6 | 32551228 | upstream gene variant | C/T | snv | 0.81 | 1 | ||
rs295340 | 1.000 | 0.040 | 6 | 159164909 | upstream gene variant | A/G | snv | 0.53 | 1 | ||
rs34411505 | 1.000 | 0.040 | 16 | 27395368 | intergenic variant | A/C;G | snv | 1 | |||
rs383592 | 1.000 | 0.040 | 8 | 89792100 | downstream gene variant | C/T | snv | 0.58 | 1 | ||
rs40457 | 1.000 | 0.040 | 8 | 89811459 | intergenic variant | A/G | snv | 0.58 | 1 | ||
rs55894533 | 1.000 | 0.040 | 8 | 11891733 | downstream gene variant | A/C;T | snv | 1 | |||
rs58600253 | 1.000 | 0.040 | 10 | 62748144 | intron variant | C/T | snv | 5.5E-02 | 1 | ||
rs6807915 | 1.000 | 0.040 | 3 | 12272347 | intergenic variant | T/C | snv | 0.65 | 1 | ||
rs6863015 | 1.000 | 0.040 | 5 | 159416227 | intron variant | C/A;T | snv | 1 | |||
rs9567307 | 1.000 | 0.040 | 13 | 43897741 | intron variant | A/G | snv | 0.27 | 1 | ||
rs2221593 | 1.000 | 0.040 | 1 | 212700089 | upstream gene variant | C/A;G;T | snv | 1 | |||
rs4720118 | 1.000 | 0.040 | 7 | 33429629 | intron variant | T/A;C | snv | 1 | |||
rs3762318 | 0.925 | 0.040 | 1 | 67131436 | intron variant | G/A | snv | 0.83 | 3 | ||
rs2024825 | 1.000 | 0.040 | 1 | 67132294 | intron variant | T/A;C;G | snv | 1 |