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rs80088139

From SNPedia

Orientationplus
Stabilizedplus
Make rs80088139(C;C)
Make rs80088139(C;G)
Make rs80088139(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position48527647
GeneFAM19A5
is asnp
is mentioned by
dbSNPrs80088139
ebirs80088139
HLIrs80088139
Exacrs80088139
Varsomers80088139
Maprs80088139
PheGenIrs80088139
hapmaprs80088139
1000 genomesrs80088139
hgdprs80088139
ensemblrs80088139
gopubmedrs80088139
geneviewrs80088139
scholarrs80088139
googlers80088139
pharmgkbrs80088139
gwascentralrs80088139
openSNPrs80088139
23andMers80088139
23andMe allrs80088139
SNP Nexus

SNPshotrs80088139
SNPdbers80088139
MSV3drs80088139
GWAS Ctlgrs80088139
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-6
Odds Ratio NR NR