rs2277923
A SNP in the NKX2-5 gene on chromosome 5. Its most notable genotype is T;T: common in clinvar
- Gene
- NKX2-5
- Location
- Chr 5173,235,021 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 49%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2277923 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageT;T 20%
- European ancestry (Utah)T;T 43%
- Han Chinese (Beijing)T;T 20%
- Japanese (Tokyo)T;T 11%
- Yoruba (Nigeria)T;T 7%
Related
Source and license
Adapted from rs2277923 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.