Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.6039389A>C | CA2013882285 | VWF | c.2443-2898T>G (n.2443-2898T>G) n.421-45455T>G | dbSNP |
12 | g.6039389A>G | CA232299784 | VWF | c.2443-2898T>C (n.2443-2898T>C) n.421-45455T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |