Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6757121 | 1.000 | 0.040 | 2 | 32224192 | 3 prime UTR variant | C/T | snv | 9.7E-02 | 1 | ||
rs376729946 | 1.000 | 0.040 | 4 | 38828732 | missense variant | C/T | snv | 1.2E-05 | 4.9E-05 | 1 | |
rs138968705 | 0.925 | 0.080 | 4 | 38828278 | missense variant | G/A | snv | 1.2E-04 | 2.3E-04 | 2 | |
rs76600635 | 0.925 | 0.040 | 4 | 38798702 | missense variant | A/G | snv | 8.2E-03 | 2.8E-03 | 3 | |
rs7194886 | 0.851 | 0.080 | 16 | 50691282 | upstream gene variant | C/T | snv | 0.38 | 4 | ||
rs5743551 | 0.742 | 0.240 | 4 | 38806033 | intron variant | T/A;C | snv | 12 | |||
rs5744168 | 0.701 | 0.480 | 1 | 223111858 | stop gained | G/A | snv | 5.3E-02 | 4.4E-02 | 18 | |
rs4833095 | 0.662 | 0.480 | 4 | 38798089 | missense variant | T/C | snv | 0.38 | 0.44 | 28 | |
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 |