| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10810666 | 1.000 | 0.120 | 9 | 16911668 | intergenic variant | C/T | snv | 0.14 | 1 | ||
| rs10962656 | 1.000 | 0.120 | 9 | 16877790 | intergenic variant | G/A | snv | 0.10 | 1 | ||
| rs4445329 | 1.000 | 0.120 | 9 | 16911759 | intergenic variant | G/A;C | snv | 1 | |||
| rs10756819 | 1.000 | 0.120 | 9 | 16858086 | intron variant | G/A;C;T | snv | 1 | |||
| rs12379183 | 1.000 | 0.120 | 9 | 16865701 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs12379687 | 1.000 | 0.120 | 9 | 16854369 | intron variant | G/A;T | snv | 1 | |||
| rs1339552 | 1.000 | 0.120 | 9 | 16848792 | intron variant | C/T | snv | 0.52 | 1 | ||
| rs1416742 | 1.000 | 0.120 | 9 | 16856885 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs4961501 | 1.000 | 0.120 | 9 | 16851680 | intron variant | T/A;C;G | snv | 1 | |||
| rs7861573 | 1.000 | 0.120 | 9 | 16862282 | intron variant | A/G;T | snv | 1 | |||
| rs121913340 | 1.000 | 0.120 | 7 | 140753379 | missense variant | C/T | snv | 1 | |||
| rs1800726 | 1.000 | 0.120 | 17 | 43070993 | missense variant | C/G;T | snv | 1 | |||
| rs1800757 | 1.000 | 0.120 | 17 | 43051069 | missense variant | G/A | snv | 1 | |||
| rs80357462 | 1.000 | 0.120 | 17 | 43057083 | missense variant | G/A;C | snv | 1 | |||
| rs56070345 | 1.000 | 0.120 | 13 | 32356497 | missense variant | G/A;C;T | snv | 6.4E-05 | 1 | ||
| rs80358479 | 1.000 | 0.120 | 13 | 32333367 | missense variant | C/T | snv | 2.1E-04 | 1.2E-04 | 1 | |
| rs80359176 | 1.000 | 0.120 | 13 | 32380076 | missense variant | C/T | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs1199923024 | 1.000 | 0.120 | 17 | 61683945 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs12937080 | 1.000 | 0.120 | 17 | 61852376 | intron variant | A/G;T | snv | 1 | |||
| rs778705666 | 1.000 | 0.120 | 17 | 2030174 | missense variant | C/T | snv | 1 | |||
| rs12938171 | 1.000 | 0.120 | 17 | 61902994 | intron variant | G/A | snv | 9.0E-03 | 1 | ||
| rs12451939 | 1.000 | 0.120 | 17 | 61970281 | intron variant | A/G | snv | 2.6E-02 | 1 | ||
| rs372000848 | 1.000 | 0.120 | 11 | 94470575 | missense variant | G/A | snv | 5.2E-05 | 7.7E-05 | 1 | |
| rs35394823 | 1.000 | 0.120 | 17 | 2040586 | missense variant | C/G | snv | 8.1E-02 | 6.8E-02 | 1 | |
| rs367899983 | 1.000 | 0.120 | 9 | 16864524 | intron variant | GTCT/- | delins | 4.2E-05 | 2 |