Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 11 | ||
rs174547 | 0.742 | 0.240 | 11 | 61803311 | intron variant | T/C | snv | 0.28 | 10 | ||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 10 | ||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 9 | |||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 | ||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs4803750 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 6 | ||
rs6982636 | 8 | 125467073 | intron variant | G/A | snv | 0.43 | 6 | ||||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
rs1160985 | 1.000 | 0.080 | 19 | 44900155 | intron variant | C/T | snv | 0.52 | 5 | ||
rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 5 | ||||
rs6754295 | 1.000 | 0.040 | 2 | 20983311 | regulatory region variant | T/G | snv | 0.27 | 5 | ||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 4 | ||||
rs4245791 | 0.882 | 0.080 | 2 | 43847292 | non coding transcript exon variant | C/A;T | snv | 4 | |||
rs6065904 | 1.000 | 0.080 | 20 | 45906012 | intron variant | G/A | snv | 0.23 | 4 | ||
rs6065906 | 20 | 45925376 | downstream gene variant | T/A;C;G | snv | 4 | |||||
rs10889353 | 1 | 62652525 | intron variant | A/C;T | snv | 3 | |||||
rs12713956 | 2 | 21018633 | intron variant | A/G | snv | 0.14 | 3 | ||||
rs331 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 3 | ||||
rs4939883 | 1.000 | 0.040 | 18 | 49640844 | TF binding site variant | T/C;G | snv | 3 | |||
rs506585 | 2 | 21174310 | intergenic variant | G/A;C;T | snv | 3 | |||||
rs17111684 | 1 | 55159875 | intron variant | C/T | snv | 3.8E-02 | 2 |