i5006087
A SNP in the CFTR gene on chromosome 7. Its most notable genotype is A;C: possible carrier of cystic fibrosis allele
- Gene
- CFTR
- Location
- Chr 7117,180,359 (GRCh38)
- Highest magnitude
- 3.1Important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;CMost notableBadpossible carrier of cystic fibrosis allele
On SNPedia: (A;C). 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
Marked as pathogenic for Cystic Fibrosis in ClinVar, but not listed at all in CFTR2 rs76879328
Source and license
Adapted from i5006087 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.