rs2122554

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(G;G)	0

Make rs2122554(A;A)

Make rs2122554(A;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

166530081

is a	snp
is	mentioned by
dbSNP	rs2122554
dbSNP (classic)	rs2122554
ClinGen	rs2122554
ebi	rs2122554
HLI	rs2122554
Exac	rs2122554
Gnomad	rs2122554
Varsome	rs2122554
LitVar	rs2122554
Map	rs2122554
PheGenI	rs2122554
Biobank	rs2122554
1000 genomes	rs2122554
hgdp	rs2122554
ensembl	rs2122554
geneview	rs2122554
scholar	rs2122554
google	rs2122554
pharmgkb	rs2122554
gwascentral	rs2122554
openSNP	rs2122554
23andMe	rs2122554
SNPshot	rs2122554
SNPdbe	rs2122554
MSV3d	rs2122554
GWAS Ctlg	rs2122554

GMAF

0.1997

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 20585324]
Trait	Conduct disorder (symptom count)
Title	Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val	0.000003
Odds Ratio	0.10 [NR] unit decrease