| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886424 | 0.776 | 0.320 | 6 | 30814225 | non coding transcript exon variant | C/T | snv | 7.1E-02 | 8.7E-02 | 4 | |
| rs1264347 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 7.9E-02 | 4 | ||
| rs115915654 | 1.000 | 0.040 | 6 | 30801949 | intron variant | C/T | snv | 2 | |||
| rs114964506 | 1.000 | 0.040 | 6 | 30814428 | non coding transcript exon variant | G/C | snv | 2 | |||
| rs1264351 | 6 | 30824340 | intron variant | G/C | snv | 7.8E-02 | 1 | ||||
| rs116396069 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 1 | |||
| rs151302046 | 6 | 30807354 | intron variant | G/A;C | snv | 1 | |||||
| rs3130783 | 1.000 | 0.040 | 6 | 30806580 | intron variant | G/A;T | snv | 1 | |||
| rs4713376 | 1.000 | 0.080 | 6 | 30805537 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs4587207 | 1.000 | 6 | 30799168 | intron variant | A/G | snv | 0.17 | 1 |