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rs16853571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16853571(A;C)
Make rs16853571(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position41751113
is asnp
is mentioned by
dbSNPrs16853571
ebirs16853571
HLIrs16853571
Exacrs16853571
Varsomers16853571
Maprs16853571
PheGenIrs16853571
hapmaprs16853571
1000 genomesrs16853571
hgdprs16853571
ensemblrs16853571
gopubmedrs16853571
geneviewrs16853571
scholarrs16853571
googlers16853571
pharmgkbrs16853571
gwascentralrs16853571
openSNPrs16853571
23andMers16853571
23andMe allrs16853571
SNP Nexus

SNPshotrs16853571
SNPdbers16853571
MSV3drs16853571
GWAS Ctlgrs16853571
GMAF0.06887
Max Magnitude0
? (A;A) (A;C) (C;C) 28

rs16853571 increases susceptibility to Crohn's disease 1.45 times for carriers of the A 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 21206965] IL23R, NOD2/CARD15, ATG16L1 and PHOX2B polymorphisms in a group of patients with Crohn's disease and correlation with sub-phenotypes


[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.