| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.38796458G>A | CA15785854 | FREM2 | c.6019+11650G>A (n.6019+11650G>A) n.6327+11650G>A n.6323+11650G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.38796458G>C | CA697925167 | FREM2 | c.6019+11650G>C (n.6019+11650G>C) n.6327+11650G>C n.6323+11650G>C | dbSNP gnomAD v3 gnomAD v4 |