Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10505474 | 0.925 | 0.080 | 8 | 127405259 | intron variant | T/C | snv | 0.47 | 3 | ||
rs12757998 | 0.925 | 0.080 | 1 | 182569343 | downstream gene variant | C/T | snv | 0.24 | 3 | ||
rs1450063773 | 0.925 | 0.080 | 19 | 50858491 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
rs16901966 | 0.925 | 0.080 | 8 | 127098007 | intron variant | A/G | snv | 0.13 | 3 | ||
rs1859962 | 0.882 | 0.160 | 17 | 71112612 | intron variant | G/T | snv | 0.56 | 3 | ||
rs266849 | 0.925 | 0.080 | 19 | 50845834 | intron variant | G/A | snv | 0.82 | 3 | ||
rs267605077 | 0.925 | 0.080 | 17 | 7675212 | missense variant | A/G;T | snv | 3 | |||
rs2707765 | 0.925 | 0.080 | 5 | 112786835 | intron variant | G/A;C;T | snv | 3 | |||
rs3747531 | 0.925 | 0.080 | 8 | 16155139 | missense variant | G/A;C | snv | 3 | |||
rs41441651 | 0.925 | 0.080 | 6 | 32396111 | missense variant | C/T | snv | 2.3E-02 | 9.5E-03 | 3 | |
rs6470517 | 0.925 | 0.080 | 8 | 127448159 | intron variant | A/G | snv | 0.15 | 3 | ||
rs1060501201 | 0.925 | 0.080 | 17 | 7674190 | missense variant | T/C;G | snv | 4 | |||
rs1197734477 | 0.925 | 0.080 | 10 | 87961012 | missense variant | A/G | snv | 4 | |||
rs137852581 | 0.882 | 0.080 | X | 67723701 | missense variant | C/T | snv | 4 | |||
rs149709822 | 0.882 | 0.080 | 19 | 50856335 | missense variant | G/A | snv | 4.0E-05 | 2.3E-04 | 4 | |
rs17632542 | 0.925 | 0.080 | 19 | 50858501 | missense variant | T/C | snv | 5.5E-02 | 4.9E-02 | 4 | |
rs1902023 | 0.882 | 0.080 | 4 | 68670366 | missense variant | A/C | snv | 0.51 | 0.53 | 4 | |
rs565453 | 0.882 | 0.160 | 5 | 112849696 | intron variant | A/C;G | snv | 4 | |||
rs822391 | 0.925 | 0.080 | 3 | 186846014 | intron variant | C/T | snv | 0.85 | 4 | ||
rs864622007 | 0.882 | 0.200 | X | 67711621 | missense variant | T/A | snv | 4 | |||
rs1042489 | 0.851 | 0.160 | 17 | 78224125 | 3 prime UTR variant | T/C | snv | 0.40 | 5 | ||
rs1290923018 | 0.851 | 0.160 | 11 | 65570699 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs1512268 | 0.851 | 0.160 | 8 | 23668950 | intergenic variant | T/C | snv | 0.50 | 5 | ||
rs2735839 | 0.827 | 0.160 | 19 | 50861367 | upstream gene variant | A/C;G | snv | 5 | |||
rs3774262 | 0.851 | 0.200 | 3 | 186854025 | intron variant | G/A | snv | 0.10 | 5 |