| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
| rs4646903 | 0.630 | 0.640 | 15 | 74719300 | downstream gene variant | A/G;T | snv | 0.18 | 36 | ||
| rs2606345 | 0.732 | 0.360 | 15 | 74724835 | intron variant | C/A | snv | 0.46 | 16 | ||
| rs1799814 | 0.807 | 0.160 | 15 | 74720646 | missense variant | G/A;T | snv | 1.6E-05; 3.1E-02 | 8 | ||
| rs1368310331 | 0.827 | 0.200 | 15 | 74723032 | synonymous variant | T/C | snv | 7.0E-06 | 6 | ||
| rs779682021 | 0.882 | 0.120 | 15 | 74721227 | missense variant | A/C | snv | 5 | |||
| rs777119337 | 0.827 | 0.200 | 15 | 74723018 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs4646422 | 0.882 | 0.120 | 15 | 74722964 | missense variant | C/T | snv | 1.1E-02 | 3.4E-03 | 5 | |
| rs2470893 | 0.882 | 0.160 | 15 | 74727108 | upstream gene variant | C/T | snv | 0.20 | 4 | ||
| rs1414323823 | 0.851 | 0.160 | 15 | 74722772 | frameshift variant | -/TCTCGGT | ins | 4.0E-06 | 4 | ||
| rs368952331 | 0.925 | 0.080 | 15 | 74722805 | missense variant | C/T | snv | 2.8E-05 | 6.3E-05 | 4 | |
| rs770140945 | 0.882 | 0.200 | 15 | 74720665 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs1279844744 | 0.925 | 0.080 | 15 | 74720521 | missense variant | A/G | snv | 3 | |||
| rs4646421 | 0.882 | 0.080 | 15 | 74723851 | intron variant | G/A;C;T | snv | 0.21 | 3 | ||
| rs766508885 | 0.925 | 0.080 | 15 | 74721321 | missense variant | G/T | snv | 2 | |||
| rs771432878 | 0.925 | 0.080 | 15 | 74723013 | missense variant | A/G | snv | 4.0E-06 | 3.5E-05 | 2 | |
| rs1376199019 | 0.925 | 0.080 | 15 | 74720557 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs755133321 | 1.000 | 0.120 | 15 | 74723072 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs56343424 | 1.000 | 0.080 | 15 | 74720496 | missense variant | C/A;T | snv | 2.1E-03; 3.3E-05 | 1 |