Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11111 | 0.882 | 0.080 | 5 | 37814000 | 3 prime UTR variant | T/C | snv | 0.22 | 5 | ||
rs6903874 | 0.851 | 0.080 | 6 | 132575771 | downstream gene variant | T/C | snv | 0.23 | 5 | ||
rs9825823 | 0.851 | 0.080 | 3 | 61096480 | intron variant | T/C | snv | 0.47 | 5 | ||
rs772659997 | 0.882 | 0.120 | 10 | 49619853 | synonymous variant | T/C | snv | 2.0E-05 | 4 | ||
rs10997871 | 0.925 | 0.080 | 10 | 67913178 | intron variant | T/C | snv | 4.1E-03 | 3 | ||
rs2412646 | 0.882 | 0.120 | 4 | 55452605 | 3 prime UTR variant | T/C | snv | 0.58 | 3 | ||
rs4658966 | 0.925 | 0.080 | 1 | 231942868 | intron variant | T/C | snv | 0.19 | 3 | ||
rs747052707 | 0.925 | 0.080 | 11 | 49192822 | missense variant | T/C | snv | 2.4E-05; 8.1E-06 | 3 | ||
rs9376026 | 0.925 | 0.080 | 6 | 134281316 | intron variant | T/C | snv | 0.43 | 3 | ||
rs7182853 | 1.000 | 0.040 | 15 | 66469947 | intron variant | T/C | snv | 0.31 | 1 | ||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs11022778 | 0.925 | 0.080 | 11 | 13369313 | intron variant | T/A;G | snv | 6 | |||
rs16139 | 0.658 | 0.560 | 7 | 24285260 | missense variant | T/A;C | snv | 4.0E-06; 3.0E-02 | 36 | ||
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 31 | |||
rs2077647 | 0.732 | 0.320 | 6 | 151807942 | synonymous variant | T/A;C | snv | 8.1E-06; 0.46 | 16 | ||
rs9470080 | 0.827 | 0.080 | 6 | 35678658 | intron variant | T/A;C | snv | 13 | |||
rs1417938 | 0.776 | 0.320 | 1 | 159714396 | intron variant | T/A;C | snv | 0.28 | 10 | ||
rs28386840 | 0.827 | 0.080 | 16 | 55652906 | upstream gene variant | T/A;C | snv | 6 | |||
rs10848635 | 0.882 | 0.080 | 12 | 2207029 | intron variant | T/A;C | snv | 0.34 | 4 | ||
rs10997875 | 0.882 | 0.080 | 10 | 67920067 | downstream gene variant | T/A;C | snv | 4 | |||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs553040076 | 0.925 | 0.080 | 19 | 10417700 | missense variant | T/A | snv | 4.5E-05 | 7.7E-05 | 3 | |
rs797045032 | 0.827 | 0.280 | 7 | 143321720 | missense variant | GG/TC | mnv | 11 | |||
rs57875989 | 0.882 | 0.080 | 1 | 7829913 | splice acceptor variant | GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC | delins | 0.11 | 0.18 | 7 | |
rs1555206402 | 0.790 | 0.320 | 11 | 119093274 | stop lost | GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- | delins | 26 |