i4000413
A SNP in the FANCC gene on chromosome 9. Its most notable genotype is D;D: Fanconi anemia
- Gene
- FANCC
- Location
- Chr 998,011,508 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- D;DMost notableBadFanconi anemia
- D;IBadcarrier of Fanconi anemia allele
- I;IGoodNo summary available.
On SNPedia: (D;D), (D;I), (I;I). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other FANCC SNPs
- i4000336A;AFanconi Anemia (FANCC-related)Very important
- i4000412A;AFanconi Anemia (FANCC-related)Very important
- rs104886456A;AFanconi Anemia (FANCC-related)Very important
- rs104886459-;-Fanconi anemiaVery important
- rs121917783A;GCarrier of a Fanconi anemia group C mutationImportant
- rs121917784A;GCarrier of a Fanconi anemia group C mutationImportant
Notes
From SNPedia
Notes
Fanconi Anemia rs104886459
Source and license
Adapted from i4000413 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.