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rs79436609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common genotype
Make rs79436609(C;C)
Make rs79436609(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position140698604
GeneTRIM42
is asnp
is mentioned by
dbSNPrs79436609
dbSNP (classic)rs79436609
ClinGenrs79436609
ebirs79436609
HLIrs79436609
Exacrs79436609
Gnomadrs79436609
Varsomers79436609
LitVarrs79436609
Maprs79436609
PheGenIrs79436609
Biobankrs79436609
1000 genomesrs79436609
hgdprs79436609
ensemblrs79436609
geneviewrs79436609
scholarrs79436609
googlers79436609
pharmgkbrs79436609
gwascentralrs79436609
openSNPrs79436609
23andMers79436609
SNPshotrs79436609
SNPdbers79436609
MSV3drs79436609
GWAS Ctlgrs79436609
Max Magnitude0
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-8
Odds Ratio NR NR