rs1800098(C;G)
From SNPedia
| unaffected carrier of an allele associated with vas deferens condition? |
| Is a | genotype |
| of | rs1800098 |
| Gene | CFTR |
| Chromosome | 7 |
| Position | 117,590,400 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;G) | 3 | unaffected carrier of an allele associated with vas deferens condition? |
| (G;G) | 0 | common in clinvar |
Prior to 2012, this genotype represented a carrier of a cystic fibrosis allele, but since 2012, the CFTR2 database annotates this as "non CF causing". It is associated in OMIM, when present in someone also carrying a bona fide CF mutation, as associated with a vas deferens condition.
