| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2904880 | 1.000 | 0.040 | 16 | 28933075 | missense variant | C/G | snv | 0.72 | 0.76 | 2 | |
| rs10220668 | 1.000 | 0.040 | 14 | 59042487 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs1035798 | 1.000 | 0.040 | 6 | 32183445 | splice region variant | G/A | snv | 0.24 | 0.19 | 1 | |
| rs11171747 | 1.000 | 0.040 | 12 | 56124624 | 3 prime UTR variant | T/A;G | snv | 1 | |||
| rs1857066 | 1.000 | 0.040 | 1 | 173363490 | non coding transcript exon variant | A/C | snv | 0.79 | 1 | ||
| rs2359661 | 1.000 | 0.040 | 16 | 31269826 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs3104398 | 1.000 | 0.040 | 6 | 32717908 | upstream gene variant | G/A | snv | 0.12 | 1 | ||
| rs3130573 | 1.000 | 0.040 | 6 | 31138491 | non coding transcript exon variant | A/C;G | snv | 8.1E-06; 0.33 | 1 | ||
| rs3790566 | 1.000 | 0.040 | 1 | 67348757 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs4342938 | 1.000 | 0.040 | 10 | 131557214 | intergenic variant | A/G | snv | 0.41 | 1 | ||
| rs4789182 | 1.000 | 0.040 | 17 | 75378864 | intron variant | G/A | snv | 0.55 | 1 | ||
| rs4941246 | 1.000 | 0.040 | 18 | 64135070 | intron variant | C/T | snv | 0.60 | 1 | ||
| rs564732150 | 1.000 | 0.040 | 6 | 31028355 | missense variant | C/T | snv | 1 | |||
| rs661968 | 1.000 | 0.040 | 15 | 33968868 | 5 prime UTR variant | C/T | snv | 0.80 | 1 | ||
| rs7190018 | 1.000 | 0.040 | 16 | 31290157 | intron variant | G/A;C | snv | 1 | |||
| rs7763822 | 1.000 | 0.040 | 6 | 33092651 | intron variant | C/T | snv | 5.4E-02 | 1 | ||
| rs7764491 | 1.000 | 0.040 | 6 | 33093063 | non coding transcript exon variant | C/G | snv | 5.4E-02 | 1 | ||
| rs7900522 | 1.000 | 0.040 | 10 | 76350213 | intron variant | T/A;C | snv | 1 | |||
| rs7934606 | 1.000 | 0.040 | 11 | 1100037 | intron variant | C/G;T | snv | 1 | |||
| rs936469 | 1.000 | 0.040 | 11 | 606749 | non coding transcript exon variant | G/A | snv | 0.24 | 1 | ||
| rs2516399 | 0.925 | 0.120 | 6 | 31513522 | upstream gene variant | A/G | snv | 0.11 | 3 | ||
| rs2523477 | 0.925 | 0.080 | 6 | 31392612 | downstream gene variant | T/C | snv | 0.10 | 3 | ||
| rs2596480 | 0.925 | 0.120 | 6 | 31458208 | intron variant | C/G;T | snv | 3 | |||
| rs3128930 | 0.925 | 0.120 | 6 | 33107889 | upstream gene variant | C/T | snv | 0.31 | 3 | ||
| rs2071295 | 0.925 | 0.120 | 6 | 32070923 | intron variant | C/T | snv | 0.25 | 2 |