| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3759222 | 1.000 | 0.040 | 12 | 91113176 | upstream gene variant | T/G | snv | 0.71 | 1 | ||
| rs3784757 | 1.000 | 0.040 | 15 | 88860173 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs3803036 | 1.000 | 0.040 | 12 | 70745884 | missense variant | T/A;C | snv | 0.77 | 1 | ||
| rs3819142 | 1.000 | 0.040 | 21 | 42137588 | missense variant | A/C | snv | 0.21 | 0.18 | 1 | |
| rs38857 | 1.000 | 0.040 | 7 | 116725359 | intron variant | T/C | snv | 0.72 | 1 | ||
| rs4764971 | 1.000 | 0.040 | 12 | 100238019 | 3 prime UTR variant | A/G | snv | 0.15 | 1 | ||
| rs4840437 | 1.000 | 0.040 | 8 | 9748754 | intron variant | G/A;T | snv | 0.58 | 1 | ||
| rs573018317 | 1.000 | 0.040 | 1 | 203499805 | missense variant | G/A | snv | 6.9E-04 | 7.7E-05 | 1 | |
| rs60542319 | 1.000 | 0.040 | 12 | 48001261 | intron variant | -/A | delins | 3.7E-04 | 1 | ||
| rs667773 | 1.000 | 0.040 | 11 | 31793814 | non coding transcript exon variant | G/A | snv | 8.5E-02 | 5.9E-02 | 1 | |
| rs6989782 | 1.000 | 0.040 | 8 | 9753028 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs7325450 | 1.000 | 0.040 | 13 | 23892865 | intron variant | A/G | snv | 0.39 | 1 | ||
| rs7331047 | 1.000 | 0.040 | 13 | 23893203 | intron variant | T/C | snv | 0.40 | 1 | ||
| rs747435661 | 1.000 | 0.040 | 10 | 84248939 | stop gained | C/A;G;T | snv | 1.6E-05; 4.8E-05; 1.2E-05 | 1 | ||
| rs747899454 | 1.000 | 0.040 | 12 | 91104193 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs754440728 | 1.000 | 0.040 | 1 | 90939706 | missense variant | C/T | snv | 4.8E-05 | 1.4E-05 | 1 | |
| rs7550232 | 1.000 | 0.040 | 1 | 218345173 | splice donor variant | A/C | snv | 0.19 | 1 | ||
| rs762724 | 1.000 | 0.040 | 5 | 178989881 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs779058448 | 1.000 | 0.040 | 6 | 47285974 | stop gained | C/A | snv | 4.0E-06 | 1 | ||
| rs954326 | 1.000 | 0.040 | 12 | 48001040 | non coding transcript exon variant | G/T | snv | 0.31 | 1 | ||
| rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
| rs2070762 | 0.925 | 0.080 | 11 | 2165105 | intron variant | A/G | snv | 0.43 | 5 | ||
| rs7084402 | 0.925 | 0.040 | 10 | 58505644 | intergenic variant | A/G | snv | 0.51 | 4 | ||
| rs1656404 | 0.925 | 0.040 | 2 | 232515231 | regulatory region variant | G/A | snv | 0.18 | 3 | ||
| rs17175798 | 0.925 | 0.040 | 15 | 79171618 | intron variant | C/A;T | snv | 3 |