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rs751728

From SNPedia

Orientationminus
Stabilizedminus
Make rs751728(A;A)
Make rs751728(A;G)
Make rs751728(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position33796256
GeneMLN
is asnp
is mentioned by
dbSNPrs751728
ebirs751728
HLIrs751728
Exacrs751728
Varsomers751728
Maprs751728
PheGenIrs751728
hapmaprs751728
1000 genomesrs751728
hgdprs751728
ensemblrs751728
gopubmedrs751728
geneviewrs751728
scholarrs751728
googlers751728
pharmgkbrs751728
gwascentralrs751728
openSNPrs751728
23andMers751728
23andMe allrs751728
SNP Nexus

SNPshotrs751728
SNPdbers751728
MSV3drs751728
GWAS Ctlgrs751728
GMAF0.438
Max Magnitude
GWAS snp
PMID [PMID 23850713]
Trait Crohn's disease
Title Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Risk Allele T
P-val 1E-8
Odds Ratio 1.32 [1.20-1.45]