rs332(TCT;TCT)

Homozygous for F508C variant of cystic fibrosis gene; benign

Is a	genotype
of	rs332
Gene	CFTR
Chromosome	7
Position	117,559,593
Merged into	Rs121909001
mentioned	by

Magnitude

0.5

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.