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rs150404479

From SNPedia

Orientationplus
Stabilizedplus
Make rs150404479(C;C)
Make rs150404479(C;T)
Make rs150404479(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position43222879
GeneCFAP57, LOC105378685
is asnp
is mentioned by
dbSNPrs150404479
dbSNP (old)rs150404479
ClinGenrs150404479
ebirs150404479
HLIrs150404479
Exacrs150404479
Gnomadrs150404479
Varsomers150404479
Maprs150404479
PheGenIrs150404479
Biobankrs150404479
1000 genomesrs150404479
hgdprs150404479
ensemblrs150404479
gopubmedrs150404479
geneviewrs150404479
scholarrs150404479
googlers150404479
pharmgkbrs150404479
gwascentralrs150404479
openSNPrs150404479
23andMers150404479
23andMe allrs150404479
SNP Nexus

SNPshotrs150404479
SNPdbers150404479
MSV3drs150404479
GWAS Ctlgrs150404479
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 1E-6
Odds Ratio NR NR