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rs8050910

From SNPedia

Orientationplus
Stabilizedplus
Make rs8050910(G;G)
Make rs8050910(G;T)
Make rs8050910(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position85105567
GeneFAM92B
is asnp
is mentioned by
dbSNPrs8050910
ebirs8050910
HLIrs8050910
Exacrs8050910
Varsomers8050910
Maprs8050910
PheGenIrs8050910
hapmaprs8050910
1000 genomesrs8050910
hgdprs8050910
ensemblrs8050910
gopubmedrs8050910
geneviewrs8050910
scholarrs8050910
googlers8050910
pharmgkbrs8050910
gwascentralrs8050910
openSNPrs8050910
23andMers8050910
23andMe allrs8050910
SNP Nexus

SNPshotrs8050910
SNPdbers8050910
MSV3drs8050910
GWAS Ctlgrs8050910
GMAF0.4348
Max Magnitude
? (G;G) (G;T) (T;T) 28
Rs8050910
PubMed [PMID 17435756OA-icon.png]
Affy Probeset SNP_A-2197527
Affy Orientation reverse
On GW 5.0 1
Alleles A/B A/C
Ancestral T
Population EU
Allele T
Case Freq. 0.61
Control Freq. 0.54
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.19
Disease Crohn's disease (CD)


rs8050910 increases susceptibility to Crohn's disease 1.19 times for carriers of the T allele [PMID 17435756OA-icon.png]


[PMID 19262523] 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

OMIM266600
DescINFLAMMATORY BOWEL DISEASE 1; IBD1
Variant
Relatedalso
[PMID 17068223OA-icon.png] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.


[PMID 18580884] Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort.