rs397508137(A;G)
From SNPedia
| CF carrier mutation, but of varying clinical consequence |
| Is a | genotype |
| of | rs397508137 |
| Gene | CFTR |
| Chromosome | 7 |
| Position | 117,540,231 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | CF carrier mutation, but of varying clinical consequence |
| (G;G) | 0 | common in clinvar |
| (G;T) | 3 | carrier of a cystic fibrosis allele |
see discussion and links via main rs-page
