{{Rsnum
|rsid=3091242
|Gene=TMEM50A
|Chromosome=1
|position=25348294
|Orientation=plus
|GMAF=0.376
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TMEM50A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 19.5 | 54.0 | 26.5
| HCB | 45.9 | 50.4 | 3.7
| JPT | 45.5 | 42.0 | 12.5
| YRI | 68.3 | 28.3 | 3.4
| ASW | 51.8 | 42.9 | 5.4
| CHB | 45.9 | 50.4 | 3.7
| CHD | 49.1 | 42.6 | 8.3
| GIH | 38.0 | 50.0 | 12.0
| LWK | 67.9 | 26.6 | 5.5
| MEX | 31.0 | 53.4 | 15.5
| MKK | 54.5 | 36.5 | 9.0
| TSI | 24.8 | 48.5 | 26.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21700265
|Trait=None
|Title=Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
|RiskAllele=
|Pval=2E-13
|OR=0.1000
|ORtxt=[NR] unit decrease
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}