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rs12000567

From SNPedia

Orientationplus
Stabilizedplus
Make rs12000567(A;A)
Make rs12000567(A;C)
Make rs12000567(C;C)
ReferenceGRCh38 38.1/142
Chromosome9
Position789499
is asnp
is mentioned by
dbSNPrs12000567
ebirs12000567
HLIrs12000567
Exacrs12000567
Varsomers12000567
Maprs12000567
PheGenIrs12000567
hapmaprs12000567
1000 genomesrs12000567
hgdprs12000567
ensemblrs12000567
gopubmedrs12000567
geneviewrs12000567
scholarrs12000567
googlers12000567
pharmgkbrs12000567
gwascentralrs12000567
openSNPrs12000567
23andMers12000567
23andMe allrs12000567
SNP Nexus

SNPshotrs12000567
SNPdbers12000567
MSV3drs12000567
GWAS Ctlgrs12000567
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24839885]
Trait Preschool internalizing problems
Title A genome-wide association meta-analysis of preschool internalizing problems.
Risk Allele A
P-val 8E-6
Odds Ratio .63 [0.35-0.91] unit increase