rs786203067(CTCA;CTCA)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs786203067 |
| Gene | SDHD |
| Chromosome | 11 |
| Position | 112,088,995 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;ACTC) | 6.2 | Hereditary PGL/PCC Syndrome |
| (CTCA;CTCA) | 0 | common in clinvar |
