| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13058338 | 1.000 | 0.040 | 22 | 37236730 | intron variant | T/A;G | snv | 4 | |||
| rs794728602 | 1.000 | 0.040 | 1 | 156115168 | missense variant | G/A | snv | 3 | |||
| rs17859821 | 1.000 | 0.040 | 16 | 55478141 | intron variant | G/A;C | snv | 0.11 | 2 | ||
| rs452159 | 1.000 | 0.040 | 20 | 44642461 | intron variant | G/T | snv | 0.28 | 2 | ||
| rs6684209 | 1.000 | 0.040 | 1 | 115707991 | intron variant | C/T | snv | 0.17 | 2 | ||
| rs7521023 | 1.000 | 0.040 | 1 | 115700759 | 3 prime UTR variant | G/A | snv | 0.64 | 2 | ||
| rs772608361 | 1.000 | 0.040 | 6 | 26087503 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs1009388 | 1.000 | 0.040 | 2 | 25168232 | intron variant | G/C | snv | 0.18 | 1 | ||
| rs1544223 | 1.000 | 0.040 | 1 | 111503935 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs200432861 | 1.000 | 0.040 | 6 | 51775844 | missense variant | G/A;C | snv | 2.4E-05; 2.0E-05 | 1 | ||
| rs3754860 | 1.000 | 0.040 | 2 | 25170385 | upstream gene variant | C/T | snv | 0.22 | 1 | ||
| rs3787429 | 1.000 | 0.040 | 20 | 62216348 | missense variant | C/G;T | snv | 4.5E-06; 0.45 | 1 | ||
| rs548787835 | 1.000 | 0.040 | 5 | 179823911 | missense variant | C/G;T | snv | 1.2E-05; 1.6E-05 | 1 | ||
| rs767312316 | 1.000 | 0.040 | 17 | 82375046 | stop gained | C/A;G;T | snv | 6.6E-05; 1.7E-05; 1.7E-05 | 1 | ||
| rs737337 | 0.925 | 0.040 | 19 | 11236817 | synonymous variant | T/C | snv | 0.15 | 0.20 | 6 | |
| rs1553265736 | 0.925 | 0.040 | 1 | 156136080 | missense variant | G/C | snv | 4 | |||
| rs198358 | 0.925 | 0.040 | 1 | 11844019 | 3 prime UTR variant | T/C | snv | 0.32 | 4 | ||
| rs1028728 | 0.925 | 0.040 | 13 | 37599679 | upstream gene variant | A/T | snv | 0.20 | 3 | ||
| rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 | ||
| rs1249958 | 0.925 | 0.040 | 12 | 54582053 | missense variant | C/T | snv | 2.7E-02 | 3 | ||
| rs1303946678 | 0.925 | 0.040 | 22 | 42126851 | missense variant | C/G | snv | 3 | |||
| rs200536955 | 0.925 | 0.040 | 19 | 35756980 | missense variant | G/A;T | snv | 7.0E-04 | 3 | ||
| rs243864 | 0.925 | 0.080 | 16 | 55478410 | intron variant | T/G | snv | 0.19 | 3 | ||
| rs3829365 | 0.925 | 0.040 | 13 | 37598759 | 5 prime UTR variant | G/A;C | snv | 4.0E-06; 0.11 | 3 | ||
| rs6026584 | 0.925 | 0.040 | 20 | 58894018 | intron variant | T/C | snv | 0.70 | 3 |