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rs150516896

From SNPedia

Orientationplus
Stabilizedplus
Make rs150516896(A;A)
Make rs150516896(A;G)
Make rs150516896(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position68561792
is asnp
is mentioned by
dbSNPrs150516896
dbSNP (old)rs150516896
ClinGenrs150516896
ebirs150516896
HLIrs150516896
Exacrs150516896
Gnomadrs150516896
Varsomers150516896
Maprs150516896
PheGenIrs150516896
Biobankrs150516896
1000 genomesrs150516896
hgdprs150516896
ensemblrs150516896
gopubmedrs150516896
geneviewrs150516896
scholarrs150516896
googlers150516896
pharmgkbrs150516896
gwascentralrs150516896
openSNPrs150516896
23andMers150516896
23andMe allrs150516896
SNP Nexus

SNPshotrs150516896
SNPdbers150516896
MSV3drs150516896
GWAS Ctlgrs150516896
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 4E-6
Odds Ratio NR NR