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rs410644

From SNPedia

Orientationplus
Stabilizedplus
Make rs410644(G;G)
Make rs410644(G;T)
Make rs410644(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position81791715
is asnp
is mentioned by
dbSNPrs410644
ebirs410644
HLIrs410644
Exacrs410644
Varsomers410644
Maprs410644
PheGenIrs410644
hapmaprs410644
1000 genomesrs410644
hgdprs410644
ensemblrs410644
gopubmedrs410644
geneviewrs410644
scholarrs410644
googlers410644
pharmgkbrs410644
gwascentralrs410644
openSNPrs410644
23andMers410644
23andMe allrs410644
SNP Nexus

SNPshotrs410644
SNPdbers410644
MSV3drs410644
GWAS Ctlgrs410644
GMAF0.3393
Max Magnitude
? (G;G) (G;T) (T;T) 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 0.000007
Odds Ratio None None