| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.6023630C>T | CA228398 | VWF | c.3379+1G>A (n.3379+1G>A) n.421-29696G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.6023630C= | CA2013874855 | VWF | c.3379+1G= (n.3379+1G=) n.421-29696G= | dbSNP |
| 12 | g.6023630C>G | CA383511759 | VWF | c.3379+1G>C (n.3379+1G>C) n.421-29696G>C | dbSNP |