rs587781266(CTCT;CTCT)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs587781266 |
| Gene | SDHB |
| Chromosome | 1 |
| Position | 17,022,654 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;CTCT) | 6.2 | Hereditary PGL/PCC Syndrome |
| (CTCT;CTCT) | 0 | common in clinvar |
