| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.37738049A>G | CA290287500 | HNF1B | c.544+1391T>C (n.544+1391T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.37738049A>C | CA2580577426 | HNF1B | c.544+1391T>G (n.544+1391T>G) | dbSNP |
| 17 | g.37738049A>T | CA2580577427 | HNF1B | c.544+1391T>A (n.544+1391T>A) | dbSNP |