rs765804978
A SNP in the HFE gene on chromosome 6. Its most notable genotype is -;CC: Carrier of a hemochromatosis variant
- Gene
- HFE
- Location
- Chr 626,091,519 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;CCMost notableBadCarrier of a hemochromatosis variant
- CC;CCGoodcommon in clinvar
On SNPedia: (-;CC), (CC;CC). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
-;CC
Unaffected in absence of a second HFE gene mutation
Source and license
Adapted from rs765804978 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.