rs448740
A SNP in the FCGR3B gene on chromosome 1. Its most notable genotype is C;T: one of the differences in NA1 and NA2 neutrophil alloantigens
- Gene
- FCGR3B
- Location
- Chr 1161,629,903 (GRCh38)
- Highest magnitude
- 0.5Typical
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadone of the differences in NA1 and NA2 neutrophil alloantigens
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in one HapMap population.
- Yoruba (Nigeria)C;T 60% T;T 0%
Notes
From SNPedia
Notes
C;T
see discussion in OMIM 610665.0001
Source and license
Adapted from rs448740 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.