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rs157640

From SNPedia

Orientationplus
Stabilizedplus
Make rs157640(G;G)
Make rs157640(G;T)
Make rs157640(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position54798000
is asnp
is mentioned by
dbSNPrs157640
dbSNP (old)rs157640
ClinGenrs157640
ebirs157640
HLIrs157640
Exacrs157640
Varsomers157640
Maprs157640
PheGenIrs157640
Biobankrs157640
1000 genomesrs157640
hgdprs157640
ensemblrs157640
gopubmedrs157640
geneviewrs157640
scholarrs157640
googlers157640
pharmgkbrs157640
gwascentralrs157640
openSNPrs157640
23andMers157640
23andMe allrs157640
SNP Nexus

SNPshotrs157640
SNPdbers157640
MSV3drs157640
GWAS Ctlgrs157640
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23936387OA-icon.png]
Trait Celiac disease
Title A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele G
P-val 5E-6
Odds Ratio NR NR