| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 13 | ||
| rs1567558314 | 0.807 | 0.080 | 17 | 10643215 | intron variant | CTGGGCATCTCTTGTGTACTTTATTTTGTAGTTACTCTTCAATGTGCCATATAGACTTCTATTTCTTCTCTACTAGACTACAAGCTCATCTGTTTTTTTCACCTGTATGTCTTGTACCTGGGAAACCTAAATATACACTTTGATGAGTGGCTATGCACTTTTTTTTTTCTTTT/- | delins | 7 | |||
| rs10510181 | 0.882 | 0.200 | 3 | 149364 | intron variant | G/A | snv | 0.31 | 4 | ||
| rs678741 | 0.851 | 0.200 | 10 | 101237824 | intron variant | G/A | snv | 0.51 | 4 | ||
| rs12432469 | 1.000 | 0.040 | 14 | 26807946 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs12432472 | 1.000 | 0.040 | 14 | 26807959 | intron variant | A/C | snv | 0.25 | 1 | ||
| rs1322330 | 1.000 | 0.040 | 10 | 101231902 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs1400180 | 1.000 | 0.040 | 3 | 129285 | intron variant | T/G | snv | 0.37 | 1 | ||
| rs1400182 | 1.000 | 0.040 | 3 | 128928 | intron variant | C/G;T | snv | 1 | |||
| rs1568097 | 1.000 | 0.040 | 3 | 138468 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs1588962 | 1.000 | 0.040 | 3 | 142352 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs1878169 | 1.000 | 0.040 | 3 | 123429 | intron variant | A/T | snv | 0.32 | 1 | ||
| rs2393069 | 1.000 | 0.040 | 10 | 56359144 | intron variant | C/G;T | snv | 1 | |||
| rs4684051 | 1.000 | 0.040 | 3 | 136842 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs594791 | 1.000 | 0.040 | 10 | 101236039 | intron variant | T/C;G | snv | 1 | |||
| rs965084 | 1.000 | 0.040 | 3 | 125415 | intron variant | G/C | snv | 0.31 | 1 | ||
| rs9819101 | 1.000 | 0.040 | 3 | 124824 | intron variant | G/A;C | snv | 0.35 | 1 | ||
| rs11190870 | 0.827 | 0.200 | 10 | 101219450 | intergenic variant | T/A;C | snv | 6 | |||
| rs200590764 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | -/T | delins | 6.6E-03 | 1 | ||
| rs76319884 | 1.000 | 0.040 | 10 | 101216249 | intergenic variant | C/G | snv | 8.8E-02 | 1 | ||
| rs7914775 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | C/T | snv | 8.8E-02 | 1 | ||
| rs11598177 | 1.000 | 0.040 | 10 | 101220399 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
| rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
| rs886040971 | 0.683 | 0.280 | 8 | 115604339 | stop gained | G/A;T | snv | 56 | |||
| rs201943194 | 0.683 | 0.480 | 7 | 21710596 | stop gained | C/T | snv | 8.5E-05 | 8.4E-05 | 38 |