| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2014486 | 1.000 | 0.040 | 11 | 1237573 | intron variant | A/G | snv | 0.52 | 2 | ||
| rs7747696 | 1.000 | 0.040 | 6 | 42093217 | non coding transcript exon variant | A/G | snv | 0.54 | 1 | ||
| rs7749023 | 1.000 | 0.040 | 6 | 42093995 | non coding transcript exon variant | A/C;T | snv | 1 | |||
| rs764097618 | 1.000 | 0.040 | 16 | 27360794 | splice donor variant | G/A | snv | 4.0E-06 | 1 | ||
| rs765803011 | 1.000 | 0.040 | 16 | 27363094 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs9315542 | 1.000 | 0.040 | 13 | 38057334 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs61516247 | 1.000 | 0.040 | 6 | 40344500 | non coding transcript exon variant | G/A | snv | 0.17 | 1 | ||
| rs1440526066 | 1.000 | 0.040 | 5 | 132679827 | missense variant | G/A | snv | 1 | |||
| rs7481521 | 1.000 | 0.040 | 11 | 1027811 | missense variant | C/T | snv | 0.50 | 0.47 | 1 | |
| rs12423190 | 1.000 | 0.040 | 12 | 112471536 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs1886753 | 1.000 | 0.040 | 6 | 40359357 | non coding transcript exon variant | C/T | snv | 0.42 | 1 |