| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4147915 | 19 | 1049306 | synonymous variant | C/A;G | snv | 0.18; 4.0E-06 | 3 | ||||
| rs12151021 | 19 | 1050875 | intron variant | A/G;T | snv | 0.69 | 3 | ||||
| rs3752246 | 1.000 | 0.080 | 19 | 1056493 | missense variant | G/C;T | snv | 0.84; 4.1E-06 | 2 | ||
| rs3752241 | 1.000 | 0.080 | 19 | 1053525 | synonymous variant | C/A;G;T | snv | 1.1E-05; 0.17; 6.9E-05 | 1 | ||
| rs3764650 | 0.790 | 0.200 | 19 | 1046521 | intron variant | T/G | snv | 0.14 | 1 | ||
| rs4147929 | 0.882 | 0.120 | 19 | 1063444 | intron variant | A/C;G | snv | 1 | |||
| rs3752231 | 1.000 | 0.080 | 19 | 1043639 | intron variant | C/A;T | snv | 1 | |||
| rs115550680 | 1.000 | 0.080 | 19 | 1050421 | intron variant | A/G | snv | 1.7E-02 | 1 | ||
| rs3795065 | 1.000 | 0.080 | 19 | 1039445 | upstream gene variant | C/G;T | snv | 1 | |||
| rs111278892 | 1.000 | 0.080 | 19 | 1039324 | upstream gene variant | C/G;T | snv | 0.12 | 1 |