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

rs16891867

From SNPedia

Orientationplus
Stabilizedplus
Make rs16891867(A;A)
Make rs16891867(A;G)
Make rs16891867(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position15395740
GeneC1QTNF7
is asnp
is mentioned by
dbSNPrs16891867
ebirs16891867
HLIrs16891867
Exacrs16891867
Varsomers16891867
Maprs16891867
PheGenIrs16891867
hapmaprs16891867
1000 genomesrs16891867
hgdprs16891867
ensemblrs16891867
gopubmedrs16891867
geneviewrs16891867
scholarrs16891867
googlers16891867
pharmgkbrs16891867
gwascentralrs16891867
openSNPrs16891867
23andMers16891867
23andMe allrs16891867
SNP Nexus

SNPshotrs16891867
SNPdbers16891867
MSV3drs16891867
GWAS Ctlgrs16891867
GMAF0.1478
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (symptom count)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 3E-9
Odds Ratio 0.15 [NR] unit increase