Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 10 | ||||
rs9977672 | 0.827 | 0.120 | 21 | 39091357 | intergenic variant | G/A | snv | 0.22 | 10 | ||
rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
rs10858740 | 12 | 88451258 | intergenic variant | A/G;T | snv | 0.56 | 5 | ||||
rs3809627 | 16 | 30091839 | 5 prime UTR variant | C/A | snv | 0.41 | 5 | ||||
rs62160676 | 2 | 111410354 | intron variant | T/C;G | snv | 5 | |||||
rs78744187 | 19 | 33263642 | intergenic variant | C/T | snv | 6.8E-02 | 5 |