| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.104783622G>A | CA10632011 | ABCA1 | c.*693C>T (n.*693C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.104783622G>C | CA1869910357 | ABCA1 | c.*693C>G (n.*693C>G) | dbSNP |
| 9 | g.104783622G= | CA1869910355 | ABCA1 | c.*693C= (n.*693C=) | dbSNP |