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rs62110082

From SNPedia

Orientationplus
Stabilizedplus
Make rs62110082(C;C)
Make rs62110082(C;T)
Make rs62110082(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51835388
is asnp
is mentioned by
dbSNPrs62110082
ebirs62110082
HLIrs62110082
Exacrs62110082
Varsomers62110082
Maprs62110082
PheGenIrs62110082
hapmaprs62110082
1000 genomesrs62110082
hgdprs62110082
ensemblrs62110082
gopubmedrs62110082
geneviewrs62110082
scholarrs62110082
googlers62110082
pharmgkbrs62110082
gwascentralrs62110082
openSNPrs62110082
23andMers62110082
23andMe allrs62110082
SNP Nexus

SNPshotrs62110082
SNPdbers62110082
MSV3drs62110082
GWAS Ctlgrs62110082
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