| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1052571 | 0.882 | 0.080 | 1 | 15524118 | missense variant | G/A | snv | 0.50 | 0.59 | 1 | |
| rs10779596 | 1 | 212903562 | downstream gene variant | G/T | snv | 0.61 | 1 | ||||
| rs10799544 | 1 | 229648978 | intron variant | T/A;C | snv | 1 | |||||
| rs10909942 | 1 | 3402205 | intron variant | C/A;G | snv | 1 | |||||
| rs11122219 | 1 | 231067843 | intergenic variant | C/T | snv | 0.18 | 1 | ||||
| rs11247763 | 1 | 28217607 | intron variant | G/T | snv | 0.19 | 1 | ||||
| rs1127818 | 1 | 25820023 | 5 prime UTR variant | G/C | snv | 0.41 | 1 | ||||
| rs11583750 | 1 | 47564678 | regulatory region variant | G/A | snv | 6.6E-02 | 1 | ||||
| rs116525159 | 1 | 3188408 | intron variant | G/A | snv | 3.2E-02 | 1 | ||||
| rs12071510 | 1 | 248877988 | intergenic variant | G/T | snv | 0.46 | 1 | ||||
| rs12121609 | 1 | 160101153 | upstream gene variant | C/T | snv | 0.28 | 1 | ||||
| rs12126043 | 1 | 147818675 | intergenic variant | G/A | snv | 0.14 | 1 | ||||
| rs12128198 | 1 | 78979853 | intron variant | C/T | snv | 7.7E-02 | 1 | ||||
| rs12136414 | 1 | 161708632 | intron variant | T/C | snv | 0.41 | 1 | ||||
| rs12136952 | 1 | 12601409 | intron variant | G/A;C | snv | 1 | |||||
| rs12138917 | 1 | 110249200 | intron variant | C/T | snv | 0.29 | 1 | ||||
| rs12142550 | 1 | 154286073 | upstream gene variant | C/T | snv | 0.21 | 1 | ||||
| rs1249090 | 1 | 47687468 | upstream gene variant | G/A | snv | 0.65 | 1 | ||||
| rs12730651 | 1 | 33289932 | intron variant | A/G | snv | 0.22 | 1 | ||||
| rs1338219 | 1 | 219624333 | intergenic variant | A/C;G;T | snv | 1 | |||||
| rs140307022 | 1 | 16043683 | upstream gene variant | -/GTCTG;TTCTG | delins | 1 | |||||
| rs146310930 | 1 | 198612161 | intergenic variant | C/T | snv | 3.2E-02 | 1 | ||||
| rs1466 | 1 | 217262839 | intergenic variant | C/T | snv | 0.13 | 1 | ||||
| rs1472226 | 1 | 212229238 | intron variant | G/A | snv | 0.51 | 1 | ||||
| rs147350405 | 1 | 154950123 | intron variant | C/A;G | snv | 2.9E-02 | 1 |