rs77834169
A SNP in the CFTR gene on chromosome 7. Its most notable genotype is C;T: carrier of a cystic fibrosis allele
- Gene
- CFTR
- Location
- Chr 7117,530,974 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadcarrier of a cystic fibrosis allele
On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other CFTR SNPs
- i4000292D;Dcystic fibrosisVery important
- rs74551128A;ACystic fibrosisVery important
- rs113993960-;-Cystic Fibrosis; homozygote for delta F-508 mutationVery important
- rs199826652-;-Cystic Fibrosis; homozygote for delta F-508 mutationVery important
- i4000309A;ACystic FibrosisVery important
- i4000294A;ACystic FibrosisVery important
- i4000296T;TCystic FibrosisVery important
- i4000297A;ACystic FibrosisVery important
Notes
From SNPedia
Notes
Cystic fibrosis; c.349C>T, Arg117Cys or R117C named i5010836 by 23andMe, but i5010835 at this same position represents the C>G change (rather than the C>T)
C;T
Cystic fibrosis mutation carrier; unaffected unless CF mutation present on other copy of CF gene This cystic fibrosis variant, known as R117S, is reported as likely to be a pathogenic change in ClinVar.
Source and license
Adapted from rs77834169 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.