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rs116951791

From SNPedia

Orientationplus
Stabilizedplus
Make rs116951791(A;A)
Make rs116951791(A;G)
Make rs116951791(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position92207493
is asnp
is mentioned by
dbSNPrs116951791
dbSNP (old)rs116951791
ClinGenrs116951791
ebirs116951791
HLIrs116951791
Exacrs116951791
Varsomers116951791
Maprs116951791
PheGenIrs116951791
Biobankrs116951791
1000 genomesrs116951791
hgdprs116951791
ensemblrs116951791
gopubmedrs116951791
geneviewrs116951791
scholarrs116951791
googlers116951791
pharmgkbrs116951791
gwascentralrs116951791
openSNPrs116951791
23andMers116951791
23andMe allrs116951791
SNP Nexus

SNPshotrs116951791
SNPdbers116951791
MSV3drs116951791
GWAS Ctlgrs116951791
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 7E-7
Odds Ratio NR NR