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rs1568889

From SNPedia

Orientationplus
Stabilizedplus
Make rs1568889(C;C)
Make rs1568889(C;T)
Make rs1568889(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position27987916
is asnp
is mentioned by
dbSNPrs1568889
ebirs1568889
HLIrs1568889
Exacrs1568889
Varsomers1568889
Maprs1568889
PheGenIrs1568889
hapmaprs1568889
1000 genomesrs1568889
hgdprs1568889
ensemblrs1568889
gopubmedrs1568889
geneviewrs1568889
scholarrs1568889
googlers1568889
pharmgkbrs1568889
gwascentralrs1568889
openSNPrs1568889
23andMers1568889
23andMe allrs1568889
SNP Nexus

SNPshotrs1568889
SNPdbers1568889
MSV3drs1568889
GWAS Ctlgrs1568889
GMAF0.1708
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 0.000002
Odds Ratio None None