{{Rsnum
|rsid=7148590
|Gene=FNTB
|Chromosome=14
|position=65006478
|Orientation=plus
|GMAF=0.4353
|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 | 31.0 | 42.5 | 26.5
| HCB | 30.7 | 54.7 | 14.6
| JPT | 31.9 | 49.6 | 18.6
| YRI | 41.8 | 50.0 | 8.2
| ASW | 40.4 | 47.4 | 12.3
| CHB | 30.7 | 54.7 | 14.6
| CHD | 35.8 | 44.0 | 20.2
| GIH | 8.9 | 43.6 | 47.5
| LWK | 66.4 | 30.9 | 2.7
| MEX | 34.5 | 51.7 | 13.8
| MKK | 39.7 | 50.6 | 9.6
| TSI | 14.7 | 52.0 | 33.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23720494
  |Trait=Blood trace element (Zn levels)
  |Title=Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
  |RiskAllele=
  |Pval=1E-7
  |OR=.14
  |ORtxt=[0.089-0.191] unit increase
  }}

{{on chip | Illumina Human 1M}}