Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2032487 | 0.882 | 0.080 | 22 | 36299382 | intron variant | C/T | snv | 0.78 | 3 | ||
rs760336723 | 0.882 | 0.240 | 7 | 131506292 | missense variant | G/A | snv | 2.8E-05 | 5.6E-05 | 3 | |
rs538166970 | 0.925 | 0.080 | 17 | 63496920 | missense variant | G/A;C | snv | 1.6E-05; 4.0E-06 | 2 | ||
rs118203979 | 0.925 | 0.080 | 1 | 42740005 | missense variant | C/T | snv | 9.0E-05 | 2.8E-05 | 2 | |
rs3024912 | 0.925 | 0.120 | 2 | 191028361 | intron variant | A/C | snv | 0.29 | 2 | ||
rs437168 | 1.000 | 0.080 | 19 | 35843517 | synonymous variant | G/A;C | snv | 7.9E-02; 1.2E-05 | 2 | ||
rs367825197 | 0.925 | 0.080 | 7 | 131509412 | stop gained | G/A | snv | 4.0E-06 | 2 | ||
rs2285450 | 1.000 | 0.080 | 19 | 35851365 | synonymous variant | G/A | snv | 2.2E-02 | 4.1E-02 | 1 | |
rs4821481 | 1.000 | 0.080 | 22 | 36299896 | intron variant | C/T | snv | 0.78 | 1 | ||
rs200640958 | 1.000 | 0.080 | 11 | 101471303 | synonymous variant | G/A;C | snv | 8.0E-06; 1.6E-05 | 1 | ||
rs754919065 | 1.000 | 0.080 | 11 | 101504767 | missense variant | G/A | snv | 6.1E-05; 4.1E-06 | 7.0E-06 | 1 |