| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34214527 | 0.925 | 0.040 | 6 | 32046679 | intron variant | C/T | snv | 0.11 | 6 | ||
| rs13211318 | 0.925 | 0.040 | 6 | 32134903 | upstream gene variant | A/C | snv | 0.11 | 5 | ||
| rs2524123 | 0.925 | 0.040 | 6 | 31297537 | intron variant | T/C | snv | 0.34 | 5 | ||
| rs3130424 | 0.925 | 0.040 | 6 | 31250462 | intergenic variant | A/C;G;T | snv | 5 | |||
| rs9468925 | 0.851 | 0.040 | 6 | 31291060 | intron variant | G/A | snv | 0.44 | 5 | ||
| rs11966200 | 0.851 | 0.040 | 6 | 31869289 | intron variant | C/T | snv | 2.9E-02 | 4.5E-02 | 4 | |
| rs2456973 | 0.925 | 0.040 | 12 | 56023144 | intron variant | A/C;G | snv | 4 | |||
| rs11079035 | 1.000 | 0.040 | 17 | 42136994 | intron variant | G/A | snv | 0.29 | 3 | ||
| rs13208776 | 0.882 | 0.040 | 6 | 168540944 | intron variant | G/A;C | snv | 3 | |||
| rs1635168 | 1.000 | 0.040 | 15 | 28290120 | intron variant | A/C | snv | 0.77 | 3 | ||
| rs2039381 | 0.882 | 0.040 | 9 | 21481484 | stop gained | G/A | snv | 4.5E-02 | 3.7E-02 | 3 | |
| rs2273844 | 0.925 | 0.040 | 14 | 24634208 | 5 prime UTR variant | G/A | snv | 0.24 | 0.26 | 3 | |
| rs291700 | 0.925 | 0.040 | 20 | 33394043 | synonymous variant | T/C | snv | 0.64 | 0.62 | 3 | |
| rs3213758 | 0.925 | 0.040 | 16 | 53605526 | missense variant | C/T | snv | 7.3E-02 | 4.7E-02 | 3 | |
| rs4744411 | 0.925 | 0.040 | 9 | 94926763 | intron variant | G/A;C;T | snv | 3 | |||
| rs6960920 | 0.925 | 0.040 | 7 | 44376473 | downstream gene variant | G/C;T | snv | 0.37 | 3 | ||
| rs734930 | 0.925 | 0.040 | 7 | 70555174 | intron variant | T/C | snv | 0.53 | 3 | ||
| rs7758128 | 0.882 | 0.040 | 6 | 32377506 | intron variant | C/A;T | snv | 4.2E-02 | 3 | ||
| rs8192917 | 0.925 | 0.040 | 14 | 24632954 | missense variant | C/T | snv | 0.76 | 0.72 | 3 | |
| rs10503019 | 0.925 | 0.040 | 18 | 57787145 | intron variant | G/A | snv | 0.17 | 2 | ||
| rs11575993 | 0.925 | 0.040 | 6 | 159688219 | missense variant | G/A | snv | 2 | |||
| rs11593576 | 0.925 | 0.040 | 10 | 79256139 | intron variant | C/T | snv | 0.29 | 2 | ||
| rs11940117 | 0.925 | 0.040 | 4 | 10725083 | intergenic variant | C/G;T | snv | 2 | |||
| rs1265181 | 0.925 | 0.040 | 6 | 31188008 | intergenic variant | G/C | snv | 0.15 | 2 | ||
| rs1298695421 | 0.925 | 0.040 | 16 | 72060682 | missense variant | C/T | snv | 7.0E-06 | 2 |