rs16831128

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs16831128(A;G)

Make rs16831128(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

132386819

is a	snp
is	mentioned by
dbSNP	rs16831128
dbSNP (classic)	rs16831128
ClinGen	rs16831128
ebi	rs16831128
HLI	rs16831128
Exac	rs16831128
Gnomad	rs16831128
Varsome	rs16831128
LitVar	rs16831128
Map	rs16831128
PheGenI	rs16831128
Biobank	rs16831128
1000 genomes	rs16831128
hgdp	rs16831128
ensembl	rs16831128
geneview	rs16831128
scholar	rs16831128
google	rs16831128
pharmgkb	rs16831128
gwascentral	rs16831128
openSNP	rs16831128
23andMe	rs16831128
SNPshot	rs16831128
SNPdbe	rs16831128
MSV3d	rs16831128
GWAS Ctlg	rs16831128

GMAF

0.1974

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 20585324]
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]