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rs4558075

From SNPedia

Orientationplus
Stabilizedplus
Make rs4558075(C;C)
Make rs4558075(C;T)
Make rs4558075(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position6359663
is asnp
is mentioned by
dbSNPrs4558075
ebirs4558075
HLIrs4558075
Exacrs4558075
Varsomers4558075
Maprs4558075
PheGenIrs4558075
hapmaprs4558075
1000 genomesrs4558075
hgdprs4558075
ensemblrs4558075
gopubmedrs4558075
geneviewrs4558075
scholarrs4558075
googlers4558075
pharmgkbrs4558075
gwascentralrs4558075
openSNPrs4558075
23andMers4558075
23andMe allrs4558075
SNP Nexus

SNPshotrs4558075
SNPdbers4558075
MSV3drs4558075
GWAS Ctlgrs4558075
Max Magnitude
? (C;C) (C;T) (T;T) 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 2E-7
Odds Ratio 1.37 [1.22-1.54]