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rs17266958

From SNPedia

Orientationplus
Stabilizedplus
Make rs17266958(C;C)
Make rs17266958(C;T)
Make rs17266958(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position80650334
is asnp
is mentioned by
dbSNPrs17266958
ebirs17266958
HLIrs17266958
Exacrs17266958
Varsomers17266958
Maprs17266958
PheGenIrs17266958
hapmaprs17266958
1000 genomesrs17266958
hgdprs17266958
ensemblrs17266958
gopubmedrs17266958
geneviewrs17266958
scholarrs17266958
googlers17266958
pharmgkbrs17266958
gwascentralrs17266958
openSNPrs17266958
23andMers17266958
23andMe allrs17266958
SNP Nexus

SNPshotrs17266958
SNPdbers17266958
MSV3drs17266958
GWAS Ctlgrs17266958
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24839885]
Trait Preschool internalizing problems
Title A genome-wide association meta-analysis of preschool internalizing problems.
Risk Allele T
P-val 4E-6
Odds Ratio .20 [0.11-0.28] unit decrease