rs235756
A SNP in the BMP2 gene on chromosome 20. Its most notable genotype is G;G: normal
- Gene
- BMP2
- Location
- Chr 206,786,464 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 32%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GMost notableNot ratednormal
- A;GNot ratedhigher transferrin levels if rs1800562(A;A)
- A;ANot ratedhigher transferrin levels if rs1800562(A;A)
SNPedia records rs235756 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.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 15% A;G 41% A;A 44%
- European ancestry (Utah)G;G 14% A;G 44% A;A 42%
- Han Chinese (Beijing)G;G 3% A;G 23% A;A 74%
- Japanese (Tokyo)G;G 2% A;G 15% A;A 83%
- Yoruba (Nigeria)G;G 22% A;G 54% A;A 25%
- African ancestry (Southwest US)G;G 29% A;G 45% A;A 27%
- Chinese (Denver)G;G 5% A;G 27% A;A 69%
- Gujarati IndianG;G 17% A;G 39% A;A 45%
- Luhya (Kenya)G;G 20% A;G 52% A;A 28%
- Mexican ancestry (Los Angeles)G;G 16% A;G 47% A;A 38%
- Maasai (Kenya)G;G 26% A;G 51% A;A 23%
- TuscanG;G 16% A;G 50% A;A 34%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs235756, a relatively common SNP in the BMP2 gene, has been associated with higher serum transferrin levels - and presumably therefore higher risk for developing hemochromatosis - in the rare individuals who are rs1800562(A;A) homozygotes, i.e. those known as C282Y homozygotes.
Source and license
Adapted from rs235756 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.