Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1010930015 | 1.000 | 0.040 | 12 | 64460250 | missense variant | A/C | snv | 4.2E-06 | 2 | ||
rs1555202947 | 1.000 | 0.040 | 12 | 64467018 | missense variant | G/C | snv | 2 | |||
rs2227288 | 1.000 | 0.040 | 19 | 8302641 | intron variant | G/C;T | snv | 0.12 | 0.14 | 2 | |
rs35311343 | 1.000 | 0.040 | 4 | 186082575 | missense variant | C/G | snv | 1.5E-03 | 1.6E-03 | 1 | |
rs739901 | 1.000 | 0.040 | 12 | 112977858 | intron variant | C/A | snv | 0.18 | 1 | ||
rs753482575 | 1.000 | 0.040 | 4 | 186078995 | missense variant | A/T | snv | 8.0E-06 | 2.8E-05 | 1 | |
rs1799822 | 0.925 | 0.080 | 1 | 53213557 | missense variant | A/G | snv | 0.16 | 0.15 | 4 | |
rs2227283 | 0.882 | 0.080 | 6 | 102055442 | missense variant | G/A;C;T | snv | 0.40; 4.0E-06 | 3 | ||
rs1889570 | 0.882 | 0.160 | 6 | 52245936 | upstream gene variant | C/A;T | snv | 3 | |||
rs1799821 | 0.827 | 0.200 | 1 | 53210776 | missense variant | G/A | snv | 0.49 | 0.46 | 8 | |
rs2229291 | 0.827 | 0.200 | 1 | 53210729 | missense variant | T/G | snv | 2.3E-02 | 1.5E-02 | 8 | |
rs1557055311 | 0.882 | 0.200 | X | 153743220 | splice acceptor variant | G/A;C | snv | 5 | |||
rs2858870 | 0.851 | 0.280 | 6 | 32604474 | intergenic variant | T/A;C | snv | 4 | |||
rs1556620697 | 0.827 | 0.360 | X | 124365758 | splice region variant | C/G | snv | 10 | |||
rs34637584 | 0.583 | 0.480 | 12 | 40340400 | missense variant | G/A | snv | 5.3E-04 | 3.6E-04 | 78 | |
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 | |
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 |