| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.104782419C>T | CA10626126 | ABCA1 | c.*1896G>A (n.*1896G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.104782419C>G | CA1869909313 | ABCA1 | c.*1896G>C (n.*1896G>C) | dbSNP |
| 9 | g.104782419C= | CA1869909312 | ABCA1 | c.*1896G= (n.*1896G=) | dbSNP |