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rs116075389

From SNPedia

Orientationplus
Stabilizedplus
Make rs116075389(C;C)
Make rs116075389(C;T)
Make rs116075389(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position68563384
is asnp
is mentioned by
dbSNPrs116075389
dbSNP (old)rs116075389
ClinGenrs116075389
ebirs116075389
HLIrs116075389
Exacrs116075389
Varsomers116075389
Maprs116075389
PheGenIrs116075389
Biobankrs116075389
1000 genomesrs116075389
hgdprs116075389
ensemblrs116075389
gopubmedrs116075389
geneviewrs116075389
scholarrs116075389
googlers116075389
pharmgkbrs116075389
gwascentralrs116075389
openSNPrs116075389
23andMers116075389
23andMe allrs116075389
SNP Nexus

SNPshotrs116075389
SNPdbers116075389
MSV3drs116075389
GWAS Ctlgrs116075389
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 3E-6
Odds Ratio NR NR