rs10492664

Orientation

minus

Stabilized

minus

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

Make rs10492664(A;A)

Make rs10492664(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

108163877

is a	snp
is	mentioned by
dbSNP	rs10492664
dbSNP (classic)	rs10492664
ClinGen	rs10492664
ebi	rs10492664
HLI	rs10492664
Exac	rs10492664
Gnomad	rs10492664
Varsome	rs10492664
LitVar	rs10492664
Map	rs10492664
PheGenI	rs10492664
Biobank	rs10492664
1000 genomes	rs10492664
hgdp	rs10492664
ensembl	rs10492664
geneview	rs10492664
scholar	rs10492664
google	rs10492664
pharmgkb	rs10492664
gwascentral	rs10492664
openSNP	rs10492664
23andMe	rs10492664
SNPshot	rs10492664
SNPdbe	rs10492664
MSV3d	rs10492664
GWAS Ctlg	rs10492664

GMAF

0.2236

Max Magnitude

0

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

GWAS snp
PMID	[PMID 18951430]
Trait	Attention-deficit/hyperactivity disorder and conduct disorder
Title	Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
Risk Allele	C
P-val	0.000001
Odds Ratio	NR NR