{{Rsnum
|rsid=235756
|Chromosome=20
|position=6786464
|Orientation=minus
|GMAF=0.3246
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BMP2
|Gene_s=BMP2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.2 | 44.2 | 41.6
| HCB | 2.9 | 23.4 | 73.7
| JPT | 1.8 | 15.0 | 83.2
| YRI | 21.8 | 53.7 | 24.5
| ASW | 28.6 | 44.6 | 26.8
| CHB | 2.9 | 23.4 | 73.7
| CHD | 4.6 | 26.6 | 68.8
| GIH | 16.8 | 38.6 | 44.6
| LWK | 20.0 | 51.8 | 28.2
| MEX | 15.5 | 46.6 | 37.9
| MKK | 25.6 | 51.3 | 23.1
| TSI | 15.7 | 50.0 | 34.3
| HapMapRevision=28
}}[[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.{{PMID|17847004|OA=1
}}

{{ neighbor
| rsid = 235754
| distance = 566
}}

{{omim
|desc=HEMOCHROMATOSIS; HFE
|id=235200
|rsnum=235756
}}

{{omim
|desc=BONE MORPHOGENETIC PROTEIN 2; BMP2
|id=112261
|rsnum=235756
}}

{{PMID Auto
|PMID=21515830
|Title=Genetic variations in the transforming growth factor beta pathway as predictors of survival in advanced non-small cell lung cancer
|OA=1
}}

{{PMID Auto
|PMID=19673882
|Title=A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
|OA=1
}}

{{PMID Auto
|PMID=19879168
|Title=A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up study.
}}

{{PMID Auto
|PMID=22323359
|Title=TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}