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rs11235667

From SNPedia

Orientationplus
Stabilizedplus
Make rs11235667(A;A)
Make rs11235667(A;G)
Make rs11235667(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position73152652
is asnp
is mentioned by
dbSNPrs11235667
ebirs11235667
HLIrs11235667
Exacrs11235667
Varsomers11235667
Maprs11235667
PheGenIrs11235667
hapmaprs11235667
1000 genomesrs11235667
hgdprs11235667
ensemblrs11235667
gopubmedrs11235667
geneviewrs11235667
scholarrs11235667
googlers11235667
pharmgkbrs11235667
gwascentralrs11235667
openSNPrs11235667
23andMers11235667
23andMe allrs11235667
SNP Nexus

SNPshotrs11235667
SNPdbers11235667
MSV3drs11235667
GWAS Ctlgrs11235667
GMAF0.02801
Max Magnitude
? (A;A) (A;G) (G;G) 28

[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 26663301] Identification of a systemic lupus erythematosus risk locus spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.