| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.172447373A>T | CA1420511380 | GHSR | c.796+245T>A (n.796+245T>A) | dbSNP |
| 3 | g.172447373A>G | CA11387164 | GHSR | c.796+245T>C (n.796+245T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.172447373A>C | CA1420511381 | GHSR | c.796+245T>G (n.796+245T>G) | dbSNP gnomAD v4 |