Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10203174 | 1.000 | 0.080 | 2 | 43462891 | intron variant | C/T | snv | 0.17 | 1 | ||
rs13405158 | 1.000 | 0.080 | 2 | 43478147 | intron variant | T/C | snv | 0.17 | 1 | ||
rs13414381 | 1.000 | 0.080 | 2 | 43340079 | intron variant | T/C | snv | 0.18 | 1 | ||
rs17334919 | 1.000 | 0.080 | 2 | 43480246 | intron variant | C/T | snv | 7.0E-02 | 1 | ||
rs35720761 | 1.000 | 0.080 | 2 | 43292838 | missense variant | C/A;G;T | snv | 2.9E-05; 9.9E-02 | 1 | ||
rs6743071 | 1.000 | 0.080 | 2 | 43359148 | intron variant | T/C;G | snv | 1 | |||
rs7578597 | 0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 | 1 |