i4000412
A SNP in the FANCC gene on chromosome 9. Its most notable genotype is A;A: Fanconi Anemia (FANCC-related)
- Gene
- FANCC
- Location
- Chr 997,864,024 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadFanconi Anemia (FANCC-related)
- A;GBadFanconi Anemia carrier
- G;GGoodnormal
On SNPedia: (A;A), (A;G), (G;G). 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
- i4000413D;DFanconi anemiaVery 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 rs104886457
A;A
Fanconi Anemia (FANCC-related)
A;G
Fanconi Anemia carrier
Source and license
Adapted from i4000412 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.