Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs116855232 | 0.742 | 0.400 | 13 | 48045719 | missense variant | C/T | snv | 2.8E-02 | 1.1E-02 | 4 | |
rs117927258 | 1.000 | 0.080 | 6 | 47108781 | intergenic variant | T/C | snv | 2.6E-04 | 2 | ||
rs145080284 | 1.000 | 0.080 | 10 | 94662973 | intergenic variant | C/G | snv | 2.8E-02 | 2 | ||
rs75466870 | 1.000 | 0.080 | 5 | 126346163 | intron variant | A/T | snv | 5.5E-03 | 2 | ||
rs78844412 | 1.000 | 0.080 | 11 | 42131190 | intron variant | T/A | snv | 8.9E-04 | 2 |