Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.35702206A>C | CA824226839 | FKBP5 | c.-20+18122T>G (n.-20+18122T>G) | dbSNP |
6 | g.35702206A>T | CA824226820 | FKBP5 | c.-20+18122T>A (n.-20+18122T>A) | dbSNP |
6 | g.35702206A>G | CA10576157 | FKBP5 | c.-20+18122T>C (n.-20+18122T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |