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rs1800098(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs1800098
GeneCFTR
Chromosome7
Position117,590,400
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;G) 3 unaffected carrier of an allele associated with vas deferens condition?
(G;G) 0 common in clinvar