Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28358278 | 0.925 | 0.080 | MT | 10400 | synonymous variant | C/T | snv | 2 | |||
rs2853826 | 0.925 | 0.080 | MT | 10398 | missense variant | A/G | snv | 2 | |||
rs41467651 | 0.925 | 0.080 | MT | 10310 | synonymous variant | G/A | snv | 2 | |||
rs1048369 | 0.882 | 0.160 | X | 133303309 | missense variant | G/A | snv | 0.33 | 0.38 | 4 | |
rs111638916 | 0.925 | 0.080 | X | 108084839 | 3 prime UTR variant | G/A | snv | 3 | |||
rs3747093 | 0.732 | 0.200 | 22 | 21630090 | upstream gene variant | G/A | snv | 0.32 | 16 | ||
rs17728461 | 0.776 | 0.120 | 22 | 30202563 | intron variant | C/G | snv | 0.25 | 9 | ||
rs12537 | 0.827 | 0.280 | 22 | 30027471 | 3 prime UTR variant | C/T | snv | 0.40 | 5 | ||
rs5999749 | 0.925 | 0.080 | 22 | 21833371 | intron variant | A/C;T | snv | 3 | |||
rs775144154 | 0.627 | 0.600 | 21 | 45531904 | missense variant | C/A;T | snv | 9.7E-06; 1.4E-05 | 38 | ||
rs4819388 | 0.790 | 0.240 | 21 | 44227538 | 3 prime UTR variant | T/C | snv | 9 | |||
rs113593938 | 0.790 | 0.200 | 21 | 44250907 | missense variant | C/T | snv | 3.5E-03 | 7 | ||
rs4998557 | 0.851 | 0.080 | 21 | 31662579 | intron variant | G/A | snv | 0.22 | 4 | ||
rs184432 | 0.882 | 0.120 | 21 | 42367453 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
rs225359 | 0.882 | 0.120 | 21 | 42367327 | upstream gene variant | G/A | snv | 0.62 | 3 | ||
rs3761376 | 0.925 | 0.080 | 21 | 42366929 | upstream gene variant | G/A | snv | 0.27 | 3 | ||
rs3814896 | 0.882 | 0.080 | 21 | 42351602 | upstream gene variant | A/G | snv | 0.17 | 3 | ||
rs9981660 | 0.882 | 0.080 | 21 | 42317828 | upstream gene variant | G/A | snv | 0.11 | 3 | ||
rs11088680 | 0.925 | 0.080 | 21 | 13514758 | upstream gene variant | A/G | snv | 0.30 | 2 | ||
rs3746444 | 0.514 | 0.760 | 20 | 34990448 | mature miRNA variant | A/G | snv | 0.20 | 0.19 | 105 | |
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs758272654 | 0.611 | 0.680 | 20 | 58909201 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 50 | |
rs2273535 | 0.645 | 0.360 | 20 | 56386485 | missense variant | A/C;T | snv | 0.28 | 38 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs2424913 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 18 |