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rs6594713

From SNPedia

Orientationplus
Stabilizedplus
Make rs6594713(A;A)
Make rs6594713(A;C)
Make rs6594713(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position113379677
GeneMCC
is asnp
is mentioned by
dbSNPrs6594713
ebirs6594713
HLIrs6594713
Exacrs6594713
Varsomers6594713
Maprs6594713
PheGenIrs6594713
hapmaprs6594713
1000 genomesrs6594713
hgdprs6594713
ensemblrs6594713
gopubmedrs6594713
geneviewrs6594713
scholarrs6594713
googlers6594713
pharmgkbrs6594713
gwascentralrs6594713
openSNPrs6594713
23andMers6594713
23andMe allrs6594713
SNP Nexus

SNPshotrs6594713
SNPdbers6594713
MSV3drs6594713
GWAS Ctlgrs6594713
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20308991]
Trait Brain cytoarchitecture
Title Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.
Risk Allele
P-val 2E-6
Odds Ratio NR NR