Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1541777 | 2 | 218722568 | intron variant | A/G | snv | 0.51 | 2 | ||||
rs1582931 | 5 | 123321505 | intergenic variant | G/A;T | snv | 2 | |||||
rs6422513 | 1 | 92566910 | intron variant | G/A;C | snv | 2 | |||||
rs6823268 | 4 | 145061411 | intron variant | A/G | snv | 0.28 | 2 | ||||
rs7195386 | 0.925 | 0.120 | 16 | 24567137 | splice region variant | T/A;C | snv | 0.56 | 2 | ||
rs7534091 | 1 | 118321993 | intergenic variant | A/G | snv | 0.23 | 2 | ||||
rs76929617 | 12 | 120429995 | intergenic variant | A/G | snv | 3.7E-02 | 2 | ||||
rs7826312 | 8 | 32542597 | intron variant | T/C | snv | 0.57 | 2 | ||||
rs9880211 | 3 | 136388707 | intron variant | G/A | snv | 0.19 | 2 |