| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11741255 | 0.724 | 0.240 | 5 | 132475490 | intron variant | G/A | snv | 0.29 | 14 | ||
| rs6894249 | 0.776 | 0.160 | 5 | 132461855 | non coding transcript exon variant | A/G | snv | 0.45 | 9 | ||
| rs17622378 | 0.790 | 0.200 | 5 | 132442760 | intron variant | A/G | snv | 0.28 | 8 | ||
| rs17622517 | 0.827 | 0.120 | 5 | 132467845 | intron variant | T/C | snv | 5.4E-02 | 5 | ||
| rs1004234 | 0.827 | 0.120 | 5 | 132421409 | intron variant | A/G;T | snv | 5 | |||
| rs3749833 | 0.925 | 0.080 | 5 | 132463934 | non coding transcript exon variant | T/C | snv | 0.23 | 4 | ||
| rs2188962 | 0.882 | 0.160 | 5 | 132435113 | intron variant | C/T | snv | 0.29 | 3 | ||
| rs6866614 | 0.925 | 0.080 | 5 | 132451445 | intron variant | A/G | snv | 0.71 | 2 | ||
| rs2548992 | 1.000 | 0.080 | 5 | 132472976 | non coding transcript exon variant | A/G;T | snv | 2 | |||
| rs12521868 | 1.000 | 0.040 | 5 | 132448701 | intron variant | G/T | snv | 0.28 | 2 | ||
| rs2522056 | 5 | 132466034 | intron variant | G/A | snv | 0.25 | 2 | ||||
| rs2248116 | 1.000 | 0.040 | 5 | 132468655 | intron variant | C/A | snv | 0.70 | 2 | ||
| rs2522061 | 5 | 132468353 | intron variant | G/T | snv | 0.24 | 2 | ||||
| rs1023518 | 1.000 | 0.080 | 5 | 132458080 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs7719499 | 5 | 132478399 | intron variant | C/G | snv | 0.37 | 1 | ||||
| rs13164856 | 1.000 | 0.120 | 5 | 132477512 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs12515180 | 5 | 132449992 | intron variant | C/T | snv | 0.28 | 1 | ||||
| rs1012793 | 5 | 132445653 | intron variant | G/A;C | snv | 1 | |||||
| rs2057655 | 5 | 132471932 | non coding transcript exon variant | G/A | snv | 0.24 | 1 | ||||
| rs2106854 | 5 | 132433482 | intron variant | C/T | snv | 0.23 | 1 | ||||
| rs7734334 | 5 | 132479312 | intron variant | C/A | snv | 0.38 | 1 | ||||
| rs6867325 | 5 | 132448313 | intron variant | A/G;T | snv | 1 | |||||
| rs2070729 | 5 | 132484229 | non coding transcript exon variant | C/A;T | snv | 0.52 | 1 | ||||
| rs10076733 | 1.000 | 0.040 | 5 | 132425039 | intron variant | G/T | snv | 0.17 | 1 | ||
| rs10900807 | 5 | 132421788 | intron variant | G/C | snv | 0.20 | 1 |