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rs2157453

From SNPedia

Orientationplus
Stabilizedplus
Make rs2157453(A;A)
Make rs2157453(A;G)
Make rs2157453(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position172894808
is asnp
is mentioned by
dbSNPrs2157453
ebirs2157453
HLIrs2157453
Exacrs2157453
Varsomers2157453
Maprs2157453
PheGenIrs2157453
hapmaprs2157453
1000 genomesrs2157453
hgdprs2157453
ensemblrs2157453
gopubmedrs2157453
geneviewrs2157453
scholarrs2157453
googlers2157453
pharmgkbrs2157453
gwascentralrs2157453
openSNPrs2157453
23andMers2157453
23andMe allrs2157453
SNP Nexus

SNPshotrs2157453
SNPdbers2157453
MSV3drs2157453
GWAS Ctlgrs2157453
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24999842OA-icon.png]
Trait Celiac disease
Title Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
Risk Allele
P-val 8E-7
Odds Ratio 1.29 [1.17–1.42]