| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2059503 | 4 | 154572267 | downstream gene variant | A/T | snv | 0.14 | 3 | ||||
| rs2227421 | 4 | 154571072 | 3 prime UTR variant | A/C | snv | 0.26 | 3 | ||||
| rs4220 | 0.925 | 0.080 | 4 | 154570607 | missense variant | G/A | snv | 0.17 | 0.15 | 3 | |
| rs6054 | 1.000 | 0.080 | 4 | 154568456 | missense variant | C/T | snv | 2.4E-03 | 2.7E-03 | 3 | |
| rs6056 | 4 | 154567669 | synonymous variant | C/T | snv | 0.17 | 0.15 | 3 | |||
| rs6058 | 4 | 154569192 | synonymous variant | G/T | snv | 5.2E-03 | 2.1E-02 | 3 | |||
| rs16844401 | 1.000 | 0.040 | 4 | 3447925 | missense variant | G/A;T | snv | 7.5E-02; 8.3E-06 | 3 | ||
| rs12712127 | 2 | 102110201 | intron variant | A/G | snv | 0.62 | 3 | ||||
| rs2106854 | 5 | 132433482 | intron variant | C/T | snv | 0.23 | 3 | ||||
| rs2522056 | 5 | 132466034 | intron variant | G/A | snv | 0.25 | 3 | ||||
| rs6874639 | 5 | 132443024 | intron variant | A/G | snv | 0.24 | 3 | ||||
| rs6873426 | 5 | 132482939 | 3 prime UTR variant | G/T | snv | 0.38 | 3 | ||||
| rs7896783 | 10 | 63402393 | intron variant | G/A;C | snv | 3 | |||||
| rs11242111 | 5 | 132420366 | intron variant | A/G;T | snv | 3 | |||||
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 3 | |||
| rs270607 | 5 | 132313493 | intron variant | A/G | snv | 0.69 | 3 | ||||
| rs7464572 | 8 | 143946999 | intron variant | C/A;G | snv | 3 | |||||
| rs10157379 | 1 | 247442297 | intron variant | C/G;T | snv | 3 | |||||
| rs1539019 | 0.882 | 0.240 | 1 | 247436999 | intron variant | A/C | snv | 0.63 | 3 | ||
| rs4925659 | 1 | 247440161 | intron variant | G/A | snv | 0.33 | 3 | ||||
| rs10512597 | 17 | 74703694 | intron variant | T/A;C | snv | 3 | |||||
| rs12915708 | 15 | 50756405 | intron variant | G/A;C | snv | 3 | |||||
| rs3091307 | 0.925 | 0.160 | 5 | 132653444 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs2286503 | 7 | 22816987 | intron variant | C/T | snv | 0.48 | 3 | ||||
| rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 4 |