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rs16831128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16831128(A;G)
Make rs16831128(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position132386819
is asnp
is mentioned by
dbSNPrs16831128
ebirs16831128
HLIrs16831128
Exacrs16831128
Varsomers16831128
Maprs16831128
PheGenIrs16831128
hapmaprs16831128
1000 genomesrs16831128
hgdprs16831128
ensemblrs16831128
gopubmedrs16831128
geneviewrs16831128
scholarrs16831128
googlers16831128
pharmgkbrs16831128
gwascentralrs16831128
openSNPrs16831128
23andMers16831128
23andMe allrs16831128
SNP Nexus

SNPshotrs16831128
SNPdbers16831128
MSV3drs16831128
GWAS Ctlgrs16831128
GMAF0.1974
Max Magnitude0
? (A;A) (A;G) (G;G) 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 4E-7
Odds Ratio 1.45 [1.26-1.67]