| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12321593 | 0.925 | 0.040 | 12 | 125129202 | non coding transcript exon variant | C/T | snv | 2.3E-02 | 2 | ||
| rs10773145 | 1.000 | 0.040 | 12 | 125141057 | non coding transcript exon variant | T/C | snv | 0.46 | 1 | ||
| rs10846834 | 1.000 | 0.040 | 12 | 125141024 | non coding transcript exon variant | A/G | snv | 0.47 | 1 | ||
| rs11058042 | 1.000 | 0.040 | 12 | 125130698 | intron variant | C/T | snv | 0.10 | 1 | ||
| rs12578446 | 1.000 | 0.040 | 12 | 125121341 | non coding transcript exon variant | A/G | snv | 0.23 | 1 | ||
| rs2297479 | 1.000 | 0.040 | 12 | 125106704 | intron variant | C/T | snv | 5.7E-02 | 1 | ||
| rs3751180 | 1.000 | 0.040 | 12 | 125142139 | synonymous variant | C/A;T | snv | 4.9E-02 | 5.1E-02 | 1 | |
| rs7136333 | 1.000 | 0.040 | 12 | 125118430 | non coding transcript exon variant | A/G | snv | 7.3E-02 | 1 | ||
| rs7970738 | 1.000 | 0.040 | 12 | 125133371 | intron variant | T/G | snv | 4.1E-02 | 1 | ||
| rs900411 | 1.000 | 0.040 | 12 | 125128293 | intron variant | G/A;C | snv | 0.33; 4.1E-06 | 1 |