Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1010023 | 0.851 | 0.080 | 22 | 43940218 | intron variant | T/C | snv | 0.20 | 4 | ||
rs7549785 | 0.925 | 0.080 | 1 | 159308078 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs12354 | 0.925 | 0.080 | 12 | 6390939 | 3 prime UTR variant | T/A;G | snv | 1.6E-04; 0.76 | 2 | ||
rs3806798 | 0.925 | 0.080 | 4 | 141636126 | upstream gene variant | T/A | snv | 8.7E-02 | 2 | ||
rs9366816 | 0.925 | 0.080 | 6 | 33136398 | intron variant | T/C | snv | 0.22 | 2 | ||
rs2617160 | 1.000 | 0.080 | 12 | 10392998 | intron variant | A/C;T | snv | 1 | |||
rs2853953 | 1.000 | 0.080 | 6 | 31267728 | downstream gene variant | G/A | snv | 0.20 | 1 | ||
rs4845384 | 1.000 | 0.080 | 1 | 154615193 | intron variant | A/G | snv | 0.69 | 1 | ||
rs4935047 | 1.000 | 0.080 | 10 | 52770307 | intron variant | A/G | snv | 0.49 | 1 | ||
rs61886277 | 1.000 | 0.080 | 10 | 94012060 | intergenic variant | C/T | snv | 0.19 | 1 | ||
rs76844316 | 1.000 | 0.080 | 3 | 112469762 | missense variant | T/G | snv | 2.4E-02 | 2.2E-02 | 1 | |
rs7712322 | 1.000 | 0.080 | 5 | 90482078 | intron variant | C/A;T | snv | 1 | |||
rs78900671 | 1.000 | 0.080 | 8 | 138653967 | intron variant | G/A;C | snv | 1 | |||
rs9287655 | 1.000 | 0.080 | 2 | 15245360 | intron variant | C/T | snv | 0.45 | 1 | ||
rs11465817 | 0.882 | 0.120 | 1 | 67255414 | intron variant | C/A;T | snv | 4 | |||
rs3759333 | 0.882 | 0.120 | 12 | 6382781 | intron variant | C/G;T | snv | 3 | |||
rs7095891 | 0.882 | 0.120 | 10 | 52771701 | upstream gene variant | G/A | snv | 0.30 | 3 | ||
rs2132039 | 0.925 | 0.120 | 4 | 69293669 | intron variant | T/A;C | snv | 2 | |||
rs3130542 | 0.827 | 0.160 | 6 | 31264334 | downstream gene variant | A/G | snv | 0.81 | 8 | ||
rs1054690270 | 0.827 | 0.160 | 8 | 144505907 | frameshift variant | CT/- | delins | 5 | |||
rs12614 | 0.851 | 0.160 | 6 | 31946402 | missense variant | C/G;T | snv | 4.1E-06; 0.12 | 5 | ||
rs200820567 | 0.882 | 0.160 | 6 | 137908903 | intergenic variant | T/A | snv | 2.0E-02 | 4 | ||
rs117648444 | 0.882 | 0.160 | 19 | 39247938 | missense variant | G/A | snv | 0.25 | 8.1E-02 | 3 | |
rs148314165 | 0.925 | 0.160 | 6 | 137908902 | intergenic variant | T/- | delins | 2.0E-02 | 3 | ||
rs3106796 | 0.882 | 0.160 | 2 | 188985047 | non coding transcript exon variant | A/G | snv | 0.35 | 3 |