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rs11195128

From SNPedia

Orientationplus
Stabilizedplus
Make rs11195128(C;C)
Make rs11195128(C;T)
Make rs11195128(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position110426390
is asnp
is mentioned by
dbSNPrs11195128
ebirs11195128
HLIrs11195128
Exacrs11195128
Varsomers11195128
Maprs11195128
PheGenIrs11195128
hapmaprs11195128
1000 genomesrs11195128
hgdprs11195128
ensemblrs11195128
gopubmedrs11195128
geneviewrs11195128
scholarrs11195128
googlers11195128
pharmgkbrs11195128
gwascentralrs11195128
openSNPrs11195128
23andMers11195128
23andMe allrs11195128
SNP Nexus

SNPshotrs11195128
SNPdbers11195128
MSV3drs11195128
GWAS Ctlgrs11195128
GMAF0.2332
Max Magnitude
? (C;C) (C;T) (T;T) 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