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rs7588591

From SNPedia

Orientationplus
Stabilizedplus
Make rs7588591(A;A)
Make rs7588591(A;C)
Make rs7588591(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position55191799
GeneCLHC1
is asnp
is mentioned by
dbSNPrs7588591
ebirs7588591
HLIrs7588591
Exacrs7588591
Varsomers7588591
Maprs7588591
PheGenIrs7588591
hapmaprs7588591
1000 genomesrs7588591
hgdprs7588591
ensemblrs7588591
gopubmedrs7588591
geneviewrs7588591
scholarrs7588591
googlers7588591
pharmgkbrs7588591
gwascentralrs7588591
openSNPrs7588591
23andMers7588591
23andMe allrs7588591
SNP Nexus

SNPshotrs7588591
SNPdbers7588591
MSV3drs7588591
GWAS Ctlgrs7588591
Max Magnitude
? (A;A) (A;C) (C;C) 28
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