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rs6844851

From SNPedia

Orientationplus
Stabilizedplus
Make rs6844851(C;C)
Make rs6844851(C;T)
Make rs6844851(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position179766847
is asnp
is mentioned by
dbSNPrs6844851
ebirs6844851
HLIrs6844851
Exacrs6844851
Varsomers6844851
Maprs6844851
PheGenIrs6844851
hapmaprs6844851
1000 genomesrs6844851
hgdprs6844851
ensemblrs6844851
gopubmedrs6844851
geneviewrs6844851
scholarrs6844851
googlers6844851
pharmgkbrs6844851
gwascentralrs6844851
openSNPrs6844851
23andMers6844851
23andMe allrs6844851
SNP Nexus

SNPshotrs6844851
SNPdbers6844851
MSV3drs6844851
GWAS Ctlgrs6844851
GMAF0.477
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 9E-7
Odds Ratio None None