| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9640883 | 0.882 | 0.120 | 7 | 134431881 | intron variant | G/A | snv | 0.21 | 4 | ||
| rs12219125 | 0.925 | 0.120 | 10 | 20304158 | intergenic variant | G/T | snv | 0.15 | 2 | ||
| rs1249719 | 1.000 | 0.120 | 9 | 114235944 | intron variant | G/A | snv | 6.8E-02 | 2 | ||
| rs3751624 | 1.000 | 0.120 | 15 | 52282973 | intron variant | C/T | snv | 0.20 | 2 | ||
| rs4462262 | 0.925 | 0.120 | 10 | 57429418 | intergenic variant | T/C | snv | 0.55 | 2 | ||
| rs9913583 | 0.925 | 0.120 | 17 | 1762036 | 5 prime UTR variant | C/A | snv | 6.6E-02 | 2 | ||
| rs1043045 | 1.000 | 0.120 | 3 | 57928451 | 3 prime UTR variant | T/C | snv | 0.31 | 1 | ||
| rs10491034 | 1.000 | 0.120 | 10 | 48602322 | intron variant | G/A;T | snv | 1 | |||
| rs1057719 | 1.000 | 0.120 | 3 | 57927987 | 3 prime UTR variant | A/G | snv | 0.31 | 1 | ||
| rs1145612 | 1.000 | 0.120 | 5 | 158271107 | upstream gene variant | C/A | snv | 0.49 | 1 | ||
| rs114790220 | 1.000 | 0.120 | 8 | 5306434 | intergenic variant | T/A;C | snv | 1 | |||
| rs11567245 | 1.000 | 0.120 | 7 | 82151406 | intron variant | T/A | snv | 1 | |||
| rs11662496 | 1.000 | 0.120 | 18 | 43695432 | intergenic variant | A/G;T | snv | 1 | |||
| rs11771617 | 1.000 | 0.120 | 7 | 125733372 | intergenic variant | A/G | snv | 0.20 | 1 | ||
| rs12150053 | 1.000 | 0.120 | 17 | 1761175 | upstream gene variant | T/A;C | snv | 1 | |||
| rs12656571 | 1.000 | 0.120 | 5 | 109742339 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs12948385 | 1.000 | 0.120 | 17 | 1761607 | upstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs13064954 | 1.000 | 0.120 | 3 | 157136953 | downstream gene variant | G/A | snv | 7.9E-02 | 1 | ||
| rs13163610 | 1.000 | 0.120 | 5 | 94213172 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs1373054855 | 1.000 | 0.120 | 17 | 64370017 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs139876191 | 1.000 | 0.120 | 6 | 34242693 | intron variant | -/C | delins | 7.7E-02; 5.8E-06 | 5.2E-02 | 1 | |
| rs140421861 | 1.000 | 0.120 | 4 | 73413512 | synonymous variant | C/T | snv | 1.1E-04 | 1.1E-04 | 1 | |
| rs142293996 | 1.000 | 0.120 | 1 | 224260357 | intron variant | C/A | snv | 1.1E-02 | 1 | ||
| rs142610219 | 1.000 | 0.120 | 8 | 115906039 | intergenic variant | A/T | snv | 2.7E-03 | 1 | ||
| rs148995025 | 1.000 | 0.120 | 5 | 7085094 | intron variant | A/G | snv | 8.9E-03 | 1 |