Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
rs5848 | 0.708 | 0.120 | 17 | 44352876 | 3 prime UTR variant | C/T | snv | 0.41 | 17 | ||
rs1223904774 | 0.790 | 0.120 | 21 | 25891772 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 8 | |
rs72824905 | 0.827 | 0.200 | 16 | 81908423 | missense variant | C/G;T | snv | 5.2E-03 | 6 | ||
rs4877365 | 0.851 | 0.120 | 9 | 87540777 | intron variant | G/A | snv | 0.28 | 4 | ||
rs4878104 | 0.851 | 0.120 | 9 | 87578076 | intron variant | C/T | snv | 0.40 | 4 | ||
rs2234256 | 0.882 | 0.120 | 6 | 41158917 | missense variant | A/G | snv | 1.8E-02 | 4.0E-02 | 3 |