| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs56807175 | 1.000 | 0.040 | 2 | 145678654 | intron variant | -/C | ins | 0.16 | 1 | ||
| rs200327371 | 1.000 | 0.040 | 2 | 148671610 | intron variant | T/- | del | 3.1E-02 | 1 | ||
| rs201447509 | 1.000 | 0.040 | 8 | 125236380 | intron variant | TC/- | del | 1 | |||
| rs70988775 | 1.000 | 0.040 | 5 | 140776321 | intergenic variant | T/- | del | 0.53 | 1 | ||
| rs138449918 | 0.882 | 0.040 | 2 | 39936810 | intron variant | AT/-;ATAT | delins | 3 | |||
| rs201048567 | 0.882 | 0.040 | 7 | 125615031 | intergenic variant | CA/- | delins | 1.0E-05 | 3 | ||
| rs10650434 | 1.000 | 0.040 | 7 | 1985461 | intron variant | -/TC | delins | 0.57 | 1 | ||
| rs11345859 | 1.000 | 0.040 | 4 | 54669212 | intron variant | CCC/-;C;CC;CCCC;CCCCC;CCCCCC | delins | 0.44 | 1 | ||
| rs11409090 | 1.000 | 0.040 | 3 | 17846143 | intron variant | -/T | delins | 0.53 | 1 | ||
| rs11439302 | 1.000 | 0.040 | 21 | 14869414 | intron variant | A/-;AA;AAA | delins | 1 | |||
| rs139425113 | 1.000 | 0.040 | 8 | 4323090 | intron variant | A/-;AA;AAA | delins | 1 | |||
| rs146678232 | 1.000 | 0.040 | 7 | 24737471 | intron variant | A/-;AA | delins | 0.15 | 1 | ||
| rs201061212 | 1.000 | 0.040 | 15 | 80091637 | intron variant | AAAA/-;AA;AAA | delins | 4.3E-05 | 1 | ||
| rs34269918 | 1.000 | 0.040 | 1 | 8364925 | intron variant | A/- | delins | 0.69 | 1 | ||
| rs34685708 | 1.000 | 0.040 | 2 | 161972220 | intron variant | A/- | delins | 0.38 | 1 | ||
| rs58033671 | 1.000 | 0.040 | 8 | 142238758 | intron variant | GCCCGCCCCTGCAC/-;GCCCGCCCCTGCACGCCCGCCCCTGCAC | delins | 1 | |||
| rs5825114 | 1.000 | 0.040 | 18 | 55081986 | intergenic variant | A/-;AA | delins | 1 | |||
| rs5891007 | 1.000 | 0.040 | 8 | 38163492 | 3 prime UTR variant | -/T | delins | 0.20 | 1 | ||
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
| rs115707823 | 0.701 | 0.320 | 6 | 30374976 | intergenic variant | G/A | snv | 19 | |||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 18 | |
| rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 18 | ||
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 16 | |
| rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 |