| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3851228 | 0.925 | 0.040 | 6 | 111526988 | intron variant | A/T | snv | 9.7E-02 | 3 | ||
| rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 3 | |
| rs6568686 | 1.000 | 0.040 | 6 | 111551279 | intron variant | T/C | snv | 0.83 | 1 | ||
| rs6568685 | 1.000 | 0.040 | 6 | 111499910 | intron variant | A/C;T | snv | 1 | |||
| rs4947121 | 6 | 111513751 | intron variant | T/C | snv | 0.72 | 1 | ||||
| rs71562294 | 0.925 | 0.080 | 6 | 111484775 | non coding transcript exon variant | A/G | snv | 1 | |||
| rs2179070 | 6 | 111564549 | intron variant | T/C;G | snv | 1 | |||||
| rs13190932 | 1.000 | 0.080 | 6 | 111591867 | missense variant | G/A | snv | 5.3E-02 | 5.0E-02 | 1 |