Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2069837 | 0.724 | 0.520 | 7 | 22728408 | intron variant | A/C;G | snv | 18 | |||
rs679620 | 0.716 | 0.360 | 11 | 102842889 | missense variant | T/C | snv | 0.58 | 0.57 | 17 | |
rs1800630 | 0.701 | 0.480 | 6 | 31574699 | upstream gene variant | C/A | snv | 0.14 | 17 | ||
rs1800972 | 0.708 | 0.440 | 8 | 6877901 | 5 prime UTR variant | C/G;T | snv | 0.79 | 16 | ||
rs2237892 | 0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 | 16 | ||
rs6354 | 0.732 | 0.280 | 17 | 30222880 | 5 prime UTR variant | G/C;T | snv | 16 | |||
rs1050501 | 0.732 | 0.440 | 1 | 161674008 | missense variant | T/C | snv | 0.16 | 0.19 | 15 | |
rs224222 | 0.724 | 0.440 | 16 | 3254463 | missense variant | C/T | snv | 0.24 | 0.21 | 15 | |
rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
rs3811463 | 0.752 | 0.400 | 1 | 26427451 | 3 prime UTR variant | T/A;C | snv | 14 | |||
rs652438 | 0.716 | 0.400 | 11 | 102865911 | missense variant | T/C;G | snv | 7.1E-02; 2.5E-04 | 14 | ||
rs2149356 | 0.742 | 0.360 | 9 | 117711921 | intron variant | T/G | snv | 0.54 | 14 | ||
rs11362 | 0.742 | 0.360 | 8 | 6877877 | 5 prime UTR variant | C/T | snv | 0.43 | 0.40 | 13 | |
rs11225395 | 0.776 | 0.360 | 11 | 102725749 | intron variant | A/C;G | snv | 11 | |||
rs1800472 | 0.752 | 0.360 | 19 | 41341955 | missense variant | G/A | snv | 2.6E-02 | 2.3E-02 | 11 | |
rs7873784 | 0.752 | 0.440 | 9 | 117716658 | 3 prime UTR variant | G/A;C;T | snv | 11 | |||
rs4612666 | 0.763 | 0.440 | 1 | 247435768 | intron variant | T/C | snv | 0.65 | 10 | ||
rs2243248 | 0.763 | 0.240 | 5 | 132672952 | upstream gene variant | T/A;C;G | snv | 9 | |||
rs9533156 | 0.807 | 0.280 | 13 | 42573535 | intron variant | T/C | snv | 0.47 | 8 | ||
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 7 | ||
rs2779249 | 0.851 | 0.200 | 17 | 27801555 | intron variant | C/A | snv | 0.33 | 7 | ||
rs6596473 | 0.807 | 0.120 | 5 | 139374887 | intron variant | G/C;T | snv | 7 | |||
rs1927907 | 0.790 | 0.320 | 9 | 117710486 | intron variant | C/T | snv | 0.18 | 7 | ||
rs2737190 | 0.827 | 0.120 | 9 | 117701903 | upstream gene variant | G/A | snv | 0.52 | 6 | ||
rs650108 | 0.827 | 0.160 | 11 | 102838056 | intron variant | G/A | snv | 0.31 | 6 |