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 | ||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 10 | ||
rs16998073 | 0.925 | 0.120 | 4 | 80263187 | upstream gene variant | A/G;T | snv | 10 | |||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs1407040 | 20 | 58897119 | intron variant | C/T | snv | 0.70 | 4 |