rs104886458
A SNP in the C9orf3 gene on chromosome 9. Its most notable genotype is G;G: Fanconi anemia
- Gene
- C9orf3
- Location
- Chr 995,101,723 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GMost notableBadFanconi anemia
- A;GBadCarrier of a Fanconi anemia mutation
- A;AGoodcommon in clinvar
SNPedia records rs104886458 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.1661T>C (p.Leu554Pro or L554P)
Source and license
Adapted from rs104886458 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.