{{Rsnum
|rsid=8050910
|Gene=FAM92B
|Chromosome=16
|position=85105567
|Orientation=plus
|GMAF=0.4348
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=FAM92B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.9 | 51.3 | 32.7
| HCB | 43.1 | 46.0 | 10.9
| JPT | 49.6 | 41.6 | 8.8
| YRI | 2.0 | 8.2 | 89.8
| ASW | 1.8 | 35.1 | 63.2
| CHB | 43.1 | 46.0 | 10.9
| CHD | 50.5 | 38.5 | 11.0
| GIH | 23.8 | 47.5 | 28.7
| LWK | 0.9 | 22.7 | 76.4
| MEX | 32.8 | 53.4 | 13.8
| MKK | 1.9 | 27.6 | 70.5
| TSI | 12.7 | 55.9 | 31.4
| HapMapRevision=28
}}{{Report GE
|PubMed=17435756
|Source=pubmed
|AffyProbeset=SNP_A-2197527
|AffyOrientation=reverse
|AlleleA=A
|AlleleB=C
|onGW5=1
|rsid=8050910
|ancestral=T
|RiskPopulation=EU
|RiskAllele=T
|CaseFreq=0.61
|ControlFreq=0.54
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.19
|Disease=Crohn's disease
|DiseaseSymbol=CD
|OA=1
}}

rs8050910 increases susceptibility to Crohn's disease 1.19 times for carriers of the T allele {{PMID|17435756|OA=1
}}

{{PMID Auto
|PMID=19262523
|Title=rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population
}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 1; IBD1
|id=266600
|rsnum=8050910
}}

{{PMID Auto
|PMID=17068223
|Title=A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
}}

{{PMID Auto
|PMID=18580884
|Title=Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}