Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 18 | |||
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 17 | |
rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 12 | ||
rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 11 | ||
rs17486278 | 0.827 | 0.120 | 15 | 78575140 | intron variant | A/C | snv | 0.32 | 9 | ||
rs12504628 | 1.000 | 0.040 | 4 | 144515172 | intron variant | T/C | snv | 0.33 | 6 | ||
rs1980057 | 1.000 | 0.040 | 4 | 144564586 | intron variant | C/T | snv | 0.31 | 6 | ||
rs13147758 | 4 | 144539078 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs8031948 | 1.000 | 0.040 | 15 | 78523715 | intron variant | G/T | snv | 0.27 | 5 |