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rs1800098(C;G)

From SNPedia

unaffected carrier of an allele associated with vas deferens condition?
Is agenotype
ofrs1800098
GeneCFTR
Chromosome7
Position117,590,400
mentionedby
Magnitude3
ReputeBad
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.