{{Rsnum
|rsid=131794
|Gene=ODF3B
|Chromosome=22
|position=50533323
|Orientation=minus
|GMAF=0.1919
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=ODF3B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 67.7 | 29.2 | 3.1
| HCB | 88.9 | 11.1 | 0.0
| JPT | 86.4 | 13.6 | 0.0
| YRI | 52.4 | 41.3 | 6.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 88.9 | 11.1 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19862010
|Trait=Mean corpuscular volume
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=A
|Pval=1E-15
|OR=0
|ORtxt=[0.003-0.005] fl decrease
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs131794
|overall_frequency_n=109
|overall_frequency_d=128
|overall_frequency=0.851562
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=92
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}