Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3810291 | 19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 | 9 | ||||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs2303108 | 19 | 47086638 | intron variant | T/C | snv | 0.63 | 3 | ||||
rs12973221 | 19 | 47111403 | intron variant | C/A | snv | 7.6E-02 | 2 | ||||
rs2241388 | 19 | 47069730 | intron variant | T/C | snv | 0.62 | 2 | ||||
rs113125564 | 19 | 47092874 | intron variant | T/C | snv | 2.9E-02 | 1 | ||||
rs17716478 | 19 | 47097336 | intron variant | C/T | snv | 5.3E-02 | 1 | ||||
rs62135070 | 19 | 47112578 | missense variant | C/T | snv | 3.7E-02 | 3.1E-02 | 1 |