| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11637249 | 1.000 | 0.040 | 15 | 73855637 | intergenic variant | T/C | snv | 0.61 | 1 | ||
| rs1452388 | 1.000 | 0.040 | 15 | 73846737 | intergenic variant | G/A | snv | 0.74 | 1 | ||
| rs1452389 | 1.000 | 0.040 | 15 | 73846481 | intergenic variant | T/C | snv | 0.61 | 1 | ||
| rs1471439 | 1.000 | 0.040 | 15 | 73814472 | intergenic variant | T/A | snv | 0.27 | 1 | ||
| rs16958382 | 1.000 | 0.040 | 15 | 73847349 | intergenic variant | A/G | snv | 5.6E-02 | 1 | ||
| rs16958390 | 1.000 | 0.040 | 15 | 73860915 | intergenic variant | T/C | snv | 6.7E-02 | 1 | ||
| rs17773784 | 1.000 | 0.040 | 15 | 73788333 | intergenic variant | T/C | snv | 0.16 | 1 | ||
| rs4338750 | 1.000 | 0.040 | 15 | 73857246 | intergenic variant | A/G | snv | 0.51 | 1 | ||
| rs4886416 | 1.000 | 0.040 | 15 | 73818655 | regulatory region variant | T/C | snv | 9.0E-02 | 1 | ||
| rs723434 | 1.000 | 0.040 | 15 | 74050989 | downstream gene variant | A/G | snv | 0.19 | 1 | ||
| rs746655 | 1.000 | 0.040 | 15 | 73815336 | intergenic variant | A/G | snv | 0.72 | 1 | ||
| rs999742 | 1.000 | 0.040 | 15 | 73823176 | TF binding site variant | G/A;T | snv | 1 | |||
| rs999743 | 1.000 | 0.040 | 15 | 73822628 | regulatory region variant | A/T | snv | 0.15 | 1 | ||
| rs4926244 | 1.000 | 0.040 | 19 | 13264099 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs3087554 | 1.000 | 0.040 | 8 | 27597925 | 3 prime UTR variant | T/C | snv | 0.23 | 0.21 | 1 | |
| rs1404699 | 1.000 | 0.040 | 7 | 147343214 | intron variant | G/A | snv | 0.64 | 1 | ||
| rs2107856 | 1.000 | 0.040 | 7 | 147491593 | intron variant | G/A;T | snv | 1 | |||
| rs7803992 | 1.000 | 0.040 | 7 | 147343905 | intron variant | A/G;T | snv | 1 | |||
| rs781952083 | 1.000 | 0.040 | 7 | 74043894 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs863223526 | 1.000 | 0.040 | 7 | 74046710 | frameshift variant | G/- | delins | 1 | |||
| rs28635903 | 1.000 | 0.040 | 15 | 22225237 | downstream gene variant | T/C | snv | 0.14 | 0.14 | 1 | |
| rs1869177 | 1.000 | 0.040 | 15 | 73868215 | downstream gene variant | G/A;T | snv | 1 | |||
| rs2290346 | 1.000 | 0.040 | 15 | 73870935 | upstream gene variant | G/A | snv | 7.2E-02 | 1 | ||
| rs12441138 | 1.000 | 0.040 | 15 | 73951556 | intron variant | G/A | snv | 5.6E-02 | 1 | ||
| rs12594472 | 1.000 | 0.040 | 15 | 73934799 | intron variant | A/T | snv | 8.4E-02 | 1 |