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rs4479806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4479806(A;A)
Make rs4479806(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position26723674
is asnp
is mentioned by
dbSNPrs4479806
dbSNP (old)rs4479806
ClinGenrs4479806
ebirs4479806
HLIrs4479806
Exacrs4479806
Varsomers4479806
Maprs4479806
PheGenIrs4479806
Biobankrs4479806
1000 genomesrs4479806
hgdprs4479806
ensemblrs4479806
gopubmedrs4479806
geneviewrs4479806
scholarrs4479806
googlers4479806
pharmgkbrs4479806
gwascentralrs4479806
openSNPrs4479806
23andMers4479806
23andMe allrs4479806
SNP Nexus

SNPshotrs4479806
SNPdbers4479806
MSV3drs4479806
GWAS Ctlgrs4479806
GMAF0.1157
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21079607OA-icon.png]
Trait
Title A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa
Risk Allele
P-val 0.000008
Odds Ratio None None