| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.6269689G>T | CA11677666 | WFS1 | c.5-7762G>T (n.5-7762G>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.6269689G>C | CA1435753596 | WFS1 | c.5-7762G>C (n.5-7762G>C) | dbSNP |
| 4 | g.6269689G>A | CA1435753595 | WFS1 | c.5-7762G>A (n.5-7762G>A) | dbSNP |