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rs12300899

From SNPedia

Orientationplus
Stabilizedplus
Make rs12300899(C;C)
Make rs12300899(C;T)
Make rs12300899(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position125062029
is asnp
is mentioned by
dbSNPrs12300899
ebirs12300899
HLIrs12300899
Exacrs12300899
Varsomers12300899
Maprs12300899
PheGenIrs12300899
hapmaprs12300899
1000 genomesrs12300899
hgdprs12300899
ensemblrs12300899
gopubmedrs12300899
geneviewrs12300899
scholarrs12300899
googlers12300899
pharmgkbrs12300899
gwascentralrs12300899
openSNPrs12300899
23andMers12300899
23andMe allrs12300899
SNP Nexus

SNPshotrs12300899
SNPdbers12300899
MSV3drs12300899
GWAS Ctlgrs12300899
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 5E-7
Odds Ratio NR NR