Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16995309 | 0.882 | 0.280 | 20 | 50581336 | missense variant | C/T | snv | 4.8E-03 | 5.0E-03 | 4 | |
rs17883901 | 0.851 | 0.240 | 6 | 53545239 | intron variant | G/A;T | snv | 6.2E-02 | 6 | ||
rs769985775 | 0.851 | 0.160 | X | 32448630 | synonymous variant | T/C | snv | 5.7E-06 | 9.5E-06 | 6 | |
rs2736654 | 0.882 | 0.120 | 6 | 38682852 | missense variant | T/A;G | snv | 4 | |||
rs7533564 | 0.925 | 0.120 | 1 | 78360228 | intron variant | C/T | snv | 0.92 | 4 | ||
rs10499298 | 6 | 155812936 | intergenic variant | C/T | snv | 0.12 | 1 | ||||
rs10499299 | 6 | 155812754 | intergenic variant | A/G | snv | 0.14 | 1 | ||||
rs17827966 | 6 | 155817575 | regulatory region variant | T/C | snv | 0.12 | 1 | ||||
rs2518344 | 6 | 101327270 | intron variant | A/G | snv | 0.62 | 1 | ||||
rs713050 | 6 | 44124392 | intron variant | T/G | snv | 0.14 | 1 |