Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs149091175 | 0.925 | 0.080 | 7 | 99863601 | stop gained | C/T | snv | 3.2E-05 | 4.2E-05 | 2 | |
rs680055 | 0.851 | 0.120 | 7 | 99859982 | missense variant | C/A;G | snv | 6.5E-02 | 0.13 | 5 | |
rs800672 | 0.925 | 0.080 | 7 | 99838575 | intron variant | G/A | snv | 0.58 | 2 | ||
rs2740574 | 0.807 | 0.360 | 7 | 99784473 | upstream gene variant | C/T | snv | 0.78 | 12 | ||
rs11902236 | 0.925 | 0.080 | 2 | 9977740 | intron variant | C/T | snv | 0.36 | 2 | ||
rs775220785 | 0.925 | 0.080 | 7 | 99772615 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
rs776746 | 0.724 | 0.400 | 7 | 99672916 | splice acceptor variant | T/C | snv | 0.72 | 21 | ||
rs1815009 | 0.925 | 0.080 | 15 | 98961442 | 3 prime UTR variant | C/T | snv | 0.65 | 3 | ||
rs2684788 | 0.925 | 0.080 | 15 | 98961208 | 3 prime UTR variant | C/T | snv | 0.51 | 2 | ||
rs12618769 | 0.882 | 0.120 | 2 | 98623468 | 3 prime UTR variant | C/T | snv | 0.18 | 3 | ||
rs2405942 | 0.925 | 0.080 | X | 9846095 | intron variant | G/A | snv | 2 | |||
rs6465657 | 0.807 | 0.280 | 7 | 98187015 | intron variant | C/T | snv | 0.41 | 0.37 | 7 | |
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1424375643 | 0.925 | 0.080 | 3 | 9751856 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs125701 | 0.790 | 0.160 | 3 | 9748794 | upstream gene variant | G/A | snv | 0.13 | 7 | ||
rs75718479 | 1.000 | 0.080 | 12 | 97483128 | intron variant | C/A | snv | 7.4E-02 | 1 | ||
rs750392184 | 0.882 | 0.160 | 1 | 9724850 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
rs2066479 | 0.790 | 0.160 | 9 | 96235528 | missense variant | C/A;G;T | snv | 7.2E-02 | 7 | ||
rs1978331 | 0.827 | 0.200 | 12 | 96015423 | intron variant | A/G | snv | 0.50 | 5 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs72552787 | 0.925 | 0.080 | 7 | 95315388 | missense variant | T/C | snv | 2 | |||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs1434536 | 0.925 | 0.080 | 4 | 95154814 | 3 prime UTR variant | C/T | snv | 0.45 | 2 | ||
rs3742330 | 0.662 | 0.640 | 14 | 95087025 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 24 | ||
rs17021918 | 0.776 | 0.240 | 4 | 94641726 | intron variant | C/T | snv | 0.30 | 8 |