{{Rsnum
|rsid=4466998
|Gene=FNTB
|Chromosome=14
|position=65008822
|Orientation=plus
|GMAF=0.4417
|Gene_s=FNTB,MAX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 23.1 | 50.0 | 26.9
| HCB | 21.1 | 57.9 | 21.1
| JPT | 33.3 | 30.8 | 35.9
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 21.1 | 57.9 | 21.1
| 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=5E-8
|OR=0
|ORtxt=[0.001-0.003] fl increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4466998
|overall_frequency_n=75
|overall_frequency_d=128
|overall_frequency=0.585938
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=66
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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