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rs74789784

From SNPedia

Orientationplus
Stabilizedplus
Make rs74789784(C;C)
Make rs74789784(C;T)
Make rs74789784(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position67804281
GeneRP11-638L3.1
is asnp
is mentioned by
dbSNPrs74789784
ebirs74789784
HLIrs74789784
Exacrs74789784
Varsomers74789784
Maprs74789784
PheGenIrs74789784
hapmaprs74789784
1000 genomesrs74789784
hgdprs74789784
ensemblrs74789784
gopubmedrs74789784
geneviewrs74789784
scholarrs74789784
googlers74789784
pharmgkbrs74789784
gwascentralrs74789784
openSNPrs74789784
23andMers74789784
23andMe allrs74789784
SNP Nexus

SNPshotrs74789784
SNPdbers74789784
MSV3drs74789784
GWAS Ctlgrs74789784
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 2E-6
Odds Ratio NR NR