Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 24 | |||||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 18 | ||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs11099098 | 0.925 | 0.120 | 4 | 80248758 | intergenic variant | G/C;T | snv | 8 | |||
rs12801636 | 1.000 | 0.040 | 11 | 65623846 | intron variant | G/A | snv | 0.25 | 5 | ||
rs62033406 | 16 | 53790314 | intron variant | A/G | snv | 0.33 | 5 | ||||
rs1407040 | 20 | 58897119 | intron variant | C/T | snv | 0.70 | 4 |