| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 13 | ||
| rs17035646 | 1 | 10736490 | intron variant | G/A;T | snv | 6 | |||||
| rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
| rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
| rs2004776 | 1 | 230712956 | intron variant | C/G;T | snv | 5 | |||||
| rs4495740 | 1 | 62658794 | intron variant | T/G | snv | 0.34 | 5 | ||||
| rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
| rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 4 | |
| rs2999159 | 1 | 112688136 | intron variant | A/G | snv | 0.85 | 4 | ||||
| rs34071855 | 1 | 10738432 | intron variant | C/G;T | snv | 4 | |||||
| rs72640287 | 1 | 11905735 | upstream gene variant | C/T | snv | 2.6E-02 | 4 | ||||
| rs12118370 | 1 | 112605645 | intron variant | A/G | snv | 0.24 | 3 | ||||
| rs12561919 | 1.000 | 0.040 | 1 | 11779866 | missense variant | C/T | snv | 0.13 | 0.13 | 3 | |
| rs149764880 | 1 | 11820674 | non coding transcript exon variant | G/T | snv | 0.14 | 3 | ||||
| rs1689788 | 1 | 182175287 | intron variant | T/C | snv | 0.29 | 3 | ||||
| rs2493141 | 1 | 230729374 | intron variant | G/A;T | snv | 3 | |||||
| rs3753581 | 1 | 11860132 | upstream gene variant | C/A;T | snv | 3 | |||||
| rs4847240 | 1 | 93352389 | intron variant | A/G | snv | 0.51 | 3 | ||||
| rs6669371 | 1 | 11822085 | intron variant | T/G | snv | 0.14 | 3 | ||||
| rs12080886 | 1 | 243222734 | intron variant | T/A;C | snv | 2 | |||||
| rs12753251 | 1 | 178560763 | upstream gene variant | G/A | snv | 0.42 | 2 | ||||
| rs13306561 | 1 | 11805747 | 5 prime UTR variant | A/G | snv | 0.18 | 2 | ||||
| rs16849553 | 1 | 229201099 | intron variant | T/C | snv | 3.7E-02 | 2 | ||||
| rs16853958 | 1 | 204559216 | downstream gene variant | A/C | snv | 0.59 | 2 |