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rs11661646

From SNPedia

Orientationplus
Stabilizedplus
Make rs11661646(C;C)
Make rs11661646(C;G)
Make rs11661646(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position67816575
GeneLOC101927430, RP11-638L3.1
is asnp
is mentioned by
dbSNPrs11661646
ebirs11661646
HLIrs11661646
Exacrs11661646
Varsomers11661646
Maprs11661646
PheGenIrs11661646
hapmaprs11661646
1000 genomesrs11661646
hgdprs11661646
ensemblrs11661646
gopubmedrs11661646
geneviewrs11661646
scholarrs11661646
googlers11661646
pharmgkbrs11661646
gwascentralrs11661646
openSNPrs11661646
23andMers11661646
23andMe allrs11661646
SNP Nexus

SNPshotrs11661646
SNPdbers11661646
MSV3drs11661646
GWAS Ctlgrs11661646
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 6E-6
Odds Ratio NR NR