rs6467(G;T)
From SNPedia
| polymorphism |
| Is a | genotype |
| of | rs6467 |
| Gene | CYP21A2 |
| Chromosome | 6 |
| Position | 32,039,081 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 3 | Carrier of allele for congenital adrenal hyperplasia |
| (C;T) | 3 | Carrier of allele for congenital adrenal hyperplasia |
| (G;G) | 0 | common in clinvar |
| (G;T) | 0 | polymorphism |
| (T;T) | 0 | common/normal |
This genotype represents a person carrying one of each of the two common (and benign) polymorphisms known for this SNP. Note which strand this SNP is defined on.
