{{Rsnum
|rsid=4809330
|Gene=ZGPAT
|Chromosome=20
|position=63718234
|Orientation=plus
|GMAF=0.3251
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZGPAT
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 11.5 | 44.2 | 44.2
| HCB | 41.5 | 45.9 | 12.6
| JPT | 36.3 | 49.6 | 14.2
| YRI | 0.0 | 4.8 | 95.2
| ASW | 3.5 | 14.0 | 82.5
| CHB | 41.5 | 45.9 | 12.6
| CHD | 42.6 | 47.2 | 10.2
| GIH | 4.0 | 27.7 | 68.3
| LWK | 0.0 | 12.3 | 87.7
| MEX | 12.1 | 29.3 | 58.6
| MKK | 1.3 | 16.2 | 82.5
| TSI | 5.9 | 37.3 | 56.9
| HapMapRevision=28
}}{{omim
|desc=INFLAMMATORY BOWEL DISEASE 24; IBD24
|id=612566
|rsnum=4809330
}}

{{PMID Auto
|PMID=20187130
|Title=Evidence of epistasis between TNFRSF14 and TNFRSF6B polymorphisms in patients with rheumatoid arthritis
}}

{{PMID Auto GWAS
|PMID=21102463
|Trait=None
|Title=Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
|RiskAllele=G
|Pval=3E-15
|OR=1.1200
|ORtxt=[1.06-1.18]
|OA=1
}}

{{PMID Auto
|PMID=20962851
|Title=Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition
}}

{{PMID Auto
|PMID=18758464
|Title=Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.
|OA=1
}}

{{PMID Auto
|PMID=19623168
|Title=Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.
}}

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