Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34500389 | 0.851 | 0.280 | 11 | 5227103 | 5 prime UTR variant | G/A;T | snv | 4 | |||
rs34598529 | 0.724 | 0.280 | 11 | 5227100 | 5 prime UTR variant | T/C | snv | 8.9E-04 | 14 | ||
rs35036378 | 0.851 | 0.200 | 14 | 64294403 | 5 prime UTR variant | A/C | snv | 7.0E-03 | 5 | ||
rs35518301 | 0.827 | 0.200 | 11 | 5234514 | 5 prime UTR variant | T/C | snv | 6 | |||
rs367732974 | 0.790 | 0.360 | 13 | 113105788 | 5 prime UTR variant | G/A | snv | 8.9E-05 | 2.8E-05 | 9 | |
rs3803662 | 0.662 | 0.440 | 16 | 52552429 | non coding transcript exon variant | A/G | snv | 0.63 | 25 | ||
rs397509430 | 0.882 | 0.200 | 11 | 5227101 | 5 prime UTR variant | A/- | del | 3 | |||
rs549591993 | 0.776 | 0.400 | 13 | 113105794 | 5 prime UTR variant | C/A | snv | 4.0E-04 | 2.8E-05 | 12 | |
rs55971303 | 0.851 | 0.120 | 17 | 43104138 | missense variant | G/T | snv | 1.0E-04 | 4.2E-05 | 4 | |
rs56187033 | 0.851 | 0.200 | 17 | 43099786 | missense variant | T/C | snv | 2.6E-04 | 2.9E-04 | 4 | |
rs562962093 | 0.742 | 0.520 | 10 | 52771740 | upstream gene variant | T/C | snv | 7.0E-06 | 13 | ||
rs63750953 | 0.790 | 0.400 | 11 | 5227097 | 5 prime UTR variant | TT/- | delins | 7.0E-06 | 10 | ||
rs6504950 | 0.807 | 0.120 | 17 | 54979110 | intron variant | G/A | snv | 0.29 | 7 | ||
rs72661131 | 0.742 | 0.480 | 10 | 52771739 | upstream gene variant | A/G | snv | 7.6E-04 | 15 | ||
rs786203411 | 0.925 | 0.120 | 13 | 32398582 | missense variant | A/G | snv | 7.0E-06 | 2 | ||
rs9282861 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 31 | |||
rs9383938 | 0.827 | 0.160 | 6 | 151666222 | intron variant | G/T | snv | 0.11 | 5 | ||
rs999737 | 0.776 | 0.200 | 14 | 68567965 | intron variant | C/T | snv | 0.16 | 8 |