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rs11235604

From SNPedia

Orientationplus
Stabilizedplus
Make rs11235604(C;C)
Make rs11235604(C;T)
Make rs11235604(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position72822491
GeneATG16L2
is asnp
is mentioned by
dbSNPrs11235604
ebirs11235604
HLIrs11235604
Exacrs11235604
Varsomers11235604
Maprs11235604
PheGenIrs11235604
hapmaprs11235604
1000 genomesrs11235604
hgdprs11235604
ensemblrs11235604
gopubmedrs11235604
geneviewrs11235604
scholarrs11235604
googlers11235604
pharmgkbrs11235604
gwascentralrs11235604
openSNPrs11235604
23andMers11235604
23andMe allrs11235604
SNP Nexus

SNPshotrs11235604
SNPdbers11235604
MSV3drs11235604
GWAS Ctlgrs11235604
GMAF0.02709
Max Magnitude

[PMID 23850713] Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations

[PMID 27611316] A functional variant of ATG16L2 is associated with Crohn's disease in the Chinese population.