{{Rsnum
|rsid=12153855
|Gene=TNXB
|Chromosome=6
|position=32107027
|Orientation=plus
|GMAF=0.1097
|Gene_s=TNXB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 2.7 | 19.5 | 77.9
| HCB | 1.5 | 12.4 | 86.1
| JPT | 0.0 | 1.8 | 98.2
| YRI | 3.4 | 40.8 | 55.8
| ASW | 5.3 | 38.6 | 56.1
| CHB | 1.5 | 12.4 | 86.1
| CHD | 0.0 | 11.0 | 89.0
| GIH | 4.0 | 33.7 | 62.4
| LWK | 0.9 | 29.1 | 70.0
| MEX | 1.7 | 6.9 | 91.4
| MKK | 1.3 | 17.9 | 80.8
| TSI | 3.9 | 20.6 | 75.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22694956
|Trait=None
|Title=Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
|RiskAllele=C
|Pval=1E-9
|OR=1.4400
|ORtxt=None
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23886662
  |Trait=Atopic dermatitis
  |Title=A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.
  |RiskAllele=T
  |Pval=3E-14
  |OR=1.58
  |ORtxt=[1.405-1.779]
  |OA=1
}}

{{PMID Auto
|PMID=15747258
|Title=A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}