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rs2699783

From SNPedia

Orientationplus
Stabilizedplus
Make rs2699783(C;C)
Make rs2699783(C;T)
Make rs2699783(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position66031567
is asnp
is mentioned by
dbSNPrs2699783
ebirs2699783
HLIrs2699783
Exacrs2699783
Varsomers2699783
Maprs2699783
PheGenIrs2699783
hapmaprs2699783
1000 genomesrs2699783
hgdprs2699783
ensemblrs2699783
gopubmedrs2699783
geneviewrs2699783
scholarrs2699783
googlers2699783
pharmgkbrs2699783
gwascentralrs2699783
openSNPrs2699783
23andMers2699783
23andMe allrs2699783
SNP Nexus

SNPshotrs2699783
SNPdbers2699783
MSV3drs2699783
GWAS Ctlgrs2699783
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 7E-6
Odds Ratio NR NR