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rs11660238

From SNPedia

Orientationplus
Stabilizedplus
Make rs11660238(C;C)
Make rs11660238(C;T)
Make rs11660238(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position67802897
GeneRP11-638L3.1
is asnp
is mentioned by
dbSNPrs11660238
ebirs11660238
HLIrs11660238
Exacrs11660238
Varsomers11660238
Maprs11660238
PheGenIrs11660238
hapmaprs11660238
1000 genomesrs11660238
hgdprs11660238
ensemblrs11660238
gopubmedrs11660238
geneviewrs11660238
scholarrs11660238
googlers11660238
pharmgkbrs11660238
gwascentralrs11660238
openSNPrs11660238
23andMers11660238
23andMe allrs11660238
SNP Nexus

SNPshotrs11660238
SNPdbers11660238
MSV3drs11660238
GWAS Ctlgrs11660238
Max Magnitude
? (C;C) (C;T) (T;T) 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