| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11692021 | 1.000 | 0.080 | 2 | 233682559 | missense variant | T/C | snv | 0.35 | 0.34 | 3 | |
| rs3729740 | 0.882 | 0.080 | 5 | 38496535 | splice acceptor variant | C/T | snv | 2.2E-02 | 8.6E-03 | 3 | |
| rs144460286 | 0.925 | 0.080 | 7 | 55155922 | missense variant | A/C | snv | 4.0E-06 | 2 | ||
| rs557806 | 1.000 | 0.080 | 19 | 48873985 | missense variant | G/A;C | snv | 1.2E-05; 0.20 | 2 | ||
| rs1023741 | 1.000 | 0.080 | 10 | 96663139 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs10920654 | 1.000 | 0.080 | 1 | 190162620 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs111861762 | 1.000 | 0.080 | 2 | 233672556 | missense variant | C/T | snv | 1.0E-04 | 3.8E-04 | 1 | |
| rs1145724 | 1.000 | 0.080 | 6 | 90477791 | intergenic variant | T/C | snv | 0.27 | 1 | ||
| rs11574077 | 1.000 | 0.080 | 12 | 47859144 | intron variant | T/C | snv | 3.3E-02 | 1 | ||
| rs11692570 | 1.000 | 0.080 | 2 | 6637860 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
| rs12949587 | 1.000 | 0.080 | 17 | 79365094 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs13402783 | 1.000 | 0.080 | 2 | 85787998 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 1 | ||
| rs1372330 | 1.000 | 0.080 | 9 | 116757309 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs1426107 | 1.000 | 0.080 | 4 | 14294676 | regulatory region variant | C/G;T | snv | 9.1E-02 | 1 | ||
| rs17053011 | 1.000 | 0.080 | 5 | 155934106 | intron variant | G/T | snv | 0.13 | 1 | ||
| rs17082301 | 1.000 | 0.080 | 4 | 53026989 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs17201864 | 1.000 | 0.080 | 15 | 88877743 | 3 prime UTR variant | C/A;T | snv | 1 | |||
| rs2163746 | 1.000 | 0.080 | 5 | 155918211 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs2327990 | 1.000 | 0.080 | 20 | 16208618 | intron variant | T/C | snv | 0.80 | 1 | ||
| rs2366964 | 1.000 | 0.080 | 3 | 59944946 | intron variant | A/G | snv | 0.16 | 1 | ||
| rs2936519 | 1.000 | 0.080 | 8 | 6781719 | non coding transcript exon variant | G/A | snv | 0.20 | 1 | ||
| rs368295543 | 1.000 | 0.080 | 4 | 15778625 | missense variant | A/G | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs3861289 | 1.000 | 0.080 | 18 | 43111710 | intron variant | C/T | snv | 9.6E-02 | 1 | ||
| rs4239258 | 1.000 | 0.080 | 17 | 7493724 | intron variant | A/G;T | snv | 1 | |||
| rs4754687 | 1.000 | 0.080 | 11 | 100559322 | intergenic variant | A/C | snv | 0.75 | 1 |