Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11753207 | 1.000 | 0.040 | 6 | 32584671 | intron variant | A/C | snv | 0.12 | 2 | ||
rs142790902 | 1.000 | 0.040 | 6 | 32582137 | intron variant | T/C | snv | 6.0E-02 | 2 | ||
rs144660248 | 1.000 | 0.040 | 6 | 32583926 | intron variant | G/T | snv | 2 | |||
rs2760981 | 1.000 | 0.040 | 6 | 32597688 | intergenic variant | G/A;C;T | snv | 2 | |||
rs28724212 | 1.000 | 0.040 | 6 | 32588824 | intron variant | A/G | snv | 2 | |||
rs41293179 | 1.000 | 0.040 | 6 | 32582101 | intron variant | C/G;T | snv | 2 | |||
rs9270074 | 1.000 | 0.040 | 6 | 32586352 | intron variant | T/C | snv | 2 |