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rs147721431

From SNPedia

Orientationplus
Stabilizedplus
Make rs147721431(C;C)
Make rs147721431(C;T)
Make rs147721431(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position93007488
is asnp
is mentioned by
dbSNPrs147721431
dbSNP (old)rs147721431
ClinGenrs147721431
ebirs147721431
HLIrs147721431
Exacrs147721431
Gnomadrs147721431
Varsomers147721431
Maprs147721431
PheGenIrs147721431
Biobankrs147721431
1000 genomesrs147721431
hgdprs147721431
ensemblrs147721431
gopubmedrs147721431
geneviewrs147721431
scholarrs147721431
googlers147721431
pharmgkbrs147721431
gwascentralrs147721431
openSNPrs147721431
23andMers147721431
23andMe allrs147721431
SNP Nexus

SNPshotrs147721431
SNPdbers147721431
MSV3drs147721431
GWAS Ctlgrs147721431
Max Magnitude
GWAS snp
PMID [PMID 24322204]
Trait Bipolar disorder (body mass index interaction)
Title Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2.
Risk Allele
P-val 1E-6
Odds Ratio NR NR