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rs4768261

From SNPedia

Orientationplus
Stabilizedplus
Make rs4768261(C;C)
Make rs4768261(C;T)
Make rs4768261(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position40441116
GeneMUC19
is asnp
is mentioned by
dbSNPrs4768261
ebirs4768261
HLIrs4768261
Exacrs4768261
Varsomers4768261
Maprs4768261
PheGenIrs4768261
hapmaprs4768261
1000 genomesrs4768261
hgdprs4768261
ensemblrs4768261
gopubmedrs4768261
geneviewrs4768261
scholarrs4768261
googlers4768261
pharmgkbrs4768261
gwascentralrs4768261
openSNPrs4768261
23andMers4768261
23andMe allrs4768261
SNP Nexus

SNPshotrs4768261
SNPdbers4768261
MSV3drs4768261
GWAS Ctlgrs4768261
GMAF0.08127
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23619718] Genome-wide Association Study Signal at the 12q12 Locus for Crohn's Disease May Represent Associations with the MUC19 Gene