Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 4 | ||
rs1063355 | 0.827 | 0.320 | 6 | 32659937 | 3 prime UTR variant | T/G | snv | 0.56 | 5 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 10 | |||
rs10995271 | 0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 | 8 | ||
rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 2 | ||
rs11175593 | 0.882 | 0.160 | 12 | 40208138 | non coding transcript exon variant | C/T | snv | 2.8E-02 | 3 | ||
rs11190140 | 0.827 | 0.160 | 10 | 99531836 | upstream gene variant | T/C | snv | 0.55 | 6 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 13 | |||
rs11236797 | 0.790 | 0.200 | 11 | 76588605 | upstream gene variant | C/A | snv | 0.39 | 8 | ||
rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 10 | |
rs11584383 | 0.827 | 0.200 | 1 | 200966738 | downstream gene variant | T/C | snv | 0.24 | 5 | ||
rs11614913 | 0.512 | 0.760 | 12 | 53991815 | mature miRNA variant | C/T | snv | 0.39 | 0.34 | 111 | |
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 7 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 18 | ||
rs13003464 | 0.827 | 0.200 | 2 | 60959694 | intron variant | A/G | snv | 0.50 | 7 | ||
rs1456893 | 0.851 | 0.160 | 7 | 50230076 | intron variant | G/A | snv | 0.69 | 4 | ||
rs1551398 | 0.882 | 0.160 | 8 | 125527809 | intron variant | G/A | snv | 0.48 | 3 | ||
rs16969968 | 0.653 | 0.360 | 15 | 78590583 | missense variant | G/A | snv | 0.26 | 0.24 | 37 | |
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 | ||
rs17293632 | 0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 | 12 | ||
rs1736135 | 0.851 | 0.160 | 21 | 15432901 | intron variant | T/C | snv | 0.33 | 4 | ||
rs174535 | 0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 | 19 | |
rs17582416 | 0.882 | 0.160 | 10 | 34998722 | regulatory region variant | T/G | snv | 0.31 | 3 |