Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 | |||
rs55872725 | 16 | 53775211 | intron variant | C/T | snv | 0.31 | 6 | ||||
rs4823006 | 22 | 29055683 | 3 prime UTR variant | A/G | snv | 0.41 | 5 | ||||
rs166840 | 17 | 19896385 | downstream gene variant | G/A | snv | 0.36 | 2 | ||||
rs2300481 | 2 | 66555335 | intron variant | C/T | snv | 0.36 | 2 |