Have questions? Visit https://www.reddit.com/r/SNPedia

rs1550057

From SNPedia

Orientationminus
Stabilizedminus
Make rs1550057(C;C)
Make rs1550057(C;T)
Make rs1550057(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position141196270
is asnp
is mentioned by
dbSNPrs1550057
ebirs1550057
HLIrs1550057
Exacrs1550057
Varsomers1550057
Maprs1550057
PheGenIrs1550057
hapmaprs1550057
1000 genomesrs1550057
hgdprs1550057
ensemblrs1550057
gopubmedrs1550057
geneviewrs1550057
scholarrs1550057
googlers1550057
pharmgkbrs1550057
gwascentralrs1550057
openSNPrs1550057
23andMers1550057
23andMe allrs1550057
SNP Nexus

SNPshotrs1550057
SNPdbers1550057
MSV3drs1550057
GWAS Ctlgrs1550057
GMAF0.3347
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (case status)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 0.000004
Odds Ratio 1.39 [1.21-1.61]