Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 50 | ||
rs1805794 | 0.605 | 0.600 | 8 | 89978251 | missense variant | C/G | snv | 0.35 | 0.31 | 41 | |
rs752021744 | 0.689 | 0.440 | 3 | 138759306 | missense variant | T/C | snv | 1.2E-05 | 29 | ||
rs2230926 | 0.662 | 0.440 | 6 | 137874929 | missense variant | T/C;G | snv | 4.0E-06; 5.4E-02 | 27 | ||
rs2239633 | 0.742 | 0.240 | 14 | 23119848 | upstream gene variant | G/A | snv | 0.38 | 12 | ||
rs3217927 | 0.827 | 0.120 | 12 | 4302638 | 3 prime UTR variant | G/A;C | snv | 5 | |||
rs1490204625 | 0.925 | 0.160 | 5 | 87268486 | missense variant | G/A | snv | 5 | |||
rs878853666 | 0.882 | 0.200 | 16 | 89803299 | missense variant | G/A | snv | 4 | |||
rs765576835 | 0.882 | 0.200 | 3 | 10036306 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
rs786202195 | 0.925 | 0.280 | 11 | 108251012 | stop gained | T/A;C;G | snv | 3 | |||
rs387906351 | 0.882 | 0.160 | 1 | 85270828 | frameshift variant | T/-;TT | delins | 3 | |||
rs4958351 | 0.882 | 0.120 | 5 | 153790814 | intron variant | G/A;T | snv | 0.31 | 3 | ||
rs199469667 | 0.925 | 0.120 | X | 71119380 | missense variant | T/G | snv | 3 | |||
rs661561 | 0.882 | 0.200 | 6 | 137876194 | intron variant | A/C | snv | 0.62 | 0.50 | 3 | |
rs398122840 | 0.925 | 0.160 | 19 | 48955714 | frameshift variant | GGGGGGG/-;GGGGGG;GGGGGGGG | delins | 2 | |||
rs1431156021 | 0.925 | 0.120 | 2 | 25243904 | missense variant | C/T | snv | 2 | |||
rs199649035 | 1.000 | 0.120 | 19 | 17838014 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
rs2307859 | 0.925 | 0.120 | 6 | 137874825 | intron variant | CCT/- | delins | 2 | |||
rs398122513 | 1.000 | 0.120 | 19 | 48955799 | missense variant | G/A | snv | 1 | |||
rs937736862 | 1.000 | 0.120 | 9 | 136496526 | stop gained | G/A | snv | 1 |