Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs312262717 | 0.790 | 0.240 | 15 | 44659104 | frameshift variant | A/-;AA | delins | 18 | |||
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 15 | |
rs1333048 | 0.683 | 0.320 | 9 | 22125348 | intron variant | A/C | snv | 0.44 | 10 | ||
rs11152369 | 0.851 | 0.040 | 18 | 55399097 | intron variant | A/C | snv | 6.3E-02 | 5 | ||
rs1054442 | 0.925 | 0.040 | 12 | 48995537 | 3 prime UTR variant | A/C | snv | 0.46 | 4 | ||
rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
rs137928907 | 0.882 | 0.040 | 12 | 130827204 | missense variant | A/C | snv | 1.4E-02 | 1.5E-02 | 3 | |
rs4380187 | 0.925 | 0.040 | 2 | 184947213 | intergenic variant | A/C | snv | 0.34 | 3 | ||
rs182107583 | 0.925 | 0.080 | 2 | 149675023 | intron variant | A/C | snv | 4.2E-03 | 2 | ||
rs7296288 | 0.851 | 0.080 | 12 | 49086185 | upstream gene variant | A/C | snv | 0.50 | 2 | ||
rs73057489 | 0.925 | 0.080 | 12 | 17370820 | regulatory region variant | A/C | snv | 3.9E-02 | 2 | ||
rs12275195 | 1.000 | 0.040 | 11 | 79394755 | intron variant | A/C | snv | 0.12 | 1 | ||
rs17826395 | 1.000 | 0.040 | 5 | 7502943 | intron variant | A/C | snv | 0.16 | 1 | ||
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs28456 | 0.925 | 0.120 | 11 | 61822009 | intron variant | A/C;G | snv | 5 | |||
rs2070615 | 1.000 | 0.040 | 12 | 48824388 | intron variant | A/C;G | snv | 4.7E-06; 0.58 | 1 | ||
rs420259 | 0.925 | 0.040 | 16 | 23622705 | intron variant | A/C;G | snv | 1 | |||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 3 | ||
rs329319 | 1.000 | 0.040 | 5 | 134570919 | intron variant | A/C;G;T | snv | 1 | |||
rs12487445 | 0.925 | 0.040 | 3 | 52584303 | intron variant | A/C;T | snv | 2 | |||
rs300774 | 0.925 | 0.040 | 2 | 112496 | intergenic variant | A/C;T | snv | 2 | |||
rs11237799 | 1.000 | 0.040 | 11 | 79356427 | intron variant | A/C;T | snv | 1 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs4447398 | 1.000 | 0.040 | 15 | 42612706 | intron variant | A/C;T | snv | 1 |