i5010738

A SNP. Its most notable genotype is A;G: possible carrier of a cystic fibrosis allele

Gene
None listed
Highest magnitude
3.0Important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableBadpossible carrier of a cystic fibrosis alleleImportant · 3.0
  2. G;GGoodcommon/normalTypical · 0.0

On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

Cystic Fibrosis rs77284892 but see also i5053835

A;G

The clinical consequence of an (A;G) genotype for this SNP is not known, however, a (G;T) SNP is a carrier for a pathogenic cystic fibrosis allele.

Source and license

Adapted from i5010738 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.