{{Rsnum
|rsid=7155454
|Gene=FNTB
|Chromosome=14
|position=65035521
|Orientation=plus
|GMAF=0.388
|Gene_s=CHURC1-FNTB,FNTB,MAX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 24.6 | 52.3 | 23.1
| HCB | 26.7 | 55.6 | 17.8
| JPT | 43.2 | 36.4 | 20.5
| YRI | 82.5 | 14.3 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.7 | 55.6 | 17.8
| 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=23222517
  |Trait=Red blood cell traits
  |Title=Seventy-five genetic loci influencing the human red blood cell.
  |RiskAllele=A
  |Pval=2E-12
  |OR=.00
  |ORtxt=[-0.00584-0.00984] unit increase
  |OA=1
}}