{{Rsnum
|rsid=9033
|Gene=B3GNT9
|Chromosome=16
|position=67148096
|Orientation=minus
|GMAF=0.4417
|Gene_s=B3GNT9,C16orf70
|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 | 19.5 | 49.6 | 31.0
| HCB | 19.7 | 45.5 | 34.8
| JPT | 13.8 | 56.0 | 30.3
| YRI | 97.2 | 2.8 | 0.0
| ASW | 71.9 | 26.3 | 1.8
| CHB | 19.7 | 45.5 | 34.8
| CHD | 16.8 | 43.0 | 40.2
| GIH | 25.3 | 50.5 | 24.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 17.2 | 41.4 | 41.4
| MKK | 85.8 | 13.5 | 0.6
| TSI | 24.8 | 48.5 | 26.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19854717
|Title=The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)
|OA=1
}}

{{PMID|18466469|OA=1
}} Genome-wide analysis of single-locus and epistasis single-nucleotide polymorphism effects on anti-cyclic citrullinated peptide as a measure of rheumatoid arthritis.

{{PMID|19503744|OA=1
}} An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.

{{PMID|19668596|OA=1
}} A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.

{{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}}