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rs332(TCT;TCT)

From SNPedia

Homozygous for F508C variant of cystic fibrosis gene; benign
Is agenotype
ofrs332
GeneCFTR
Chromosome7
Position117,559,593
Merged intoRs121909001
mentionedby
Magnitude0.5
Geno Mag Summary
(TCT;TCT) 0.5 Homozygous for F508C variant of cystic fibrosis gene; benign
(TTT;TCT) 0.5 Heterozygous for F508C variant of cystic fibrosis gene; benign
(TTT;TTT) 0 normal form

This variation, known as F508C, causes a benign change in amino acid 508 of the cystic fibrosis gene protein.