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rs6627057

From SNPedia

Orientationplus
Stabilizedplus
Make rs6627057(G;G)
Make rs6627057(G;T)
Make rs6627057(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position145059799
is asnp
is mentioned by
dbSNPrs6627057
ClinGenrs6627057
ebirs6627057
HLIrs6627057
Exacrs6627057
Varsomers6627057
Maprs6627057
PheGenIrs6627057
hapmaprs6627057
1000 genomesrs6627057
hgdprs6627057
ensemblrs6627057
gopubmedrs6627057
geneviewrs6627057
scholarrs6627057
googlers6627057
pharmgkbrs6627057
gwascentralrs6627057
openSNPrs6627057
23andMers6627057
23andMe allrs6627057
SNP Nexus

SNPshotrs6627057
SNPdbers6627057
MSV3drs6627057
GWAS Ctlgrs6627057
GMAF0.2001
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20889312]
Trait
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
Risk Allele C
P-val 0.000001
Odds Ratio 1.47 [NR]