rs10180522

Orientation

plus

Stabilized

plus

Make rs10180522(A;A)

Make rs10180522(A;C)

Make rs10180522(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

145314285

is a	snp
is	mentioned by
dbSNP	rs10180522
dbSNP (classic)	rs10180522
ClinGen	rs10180522
ebi	rs10180522
HLI	rs10180522
Exac	rs10180522
Gnomad	rs10180522
Varsome	rs10180522
LitVar	rs10180522
Map	rs10180522
PheGenI	rs10180522
Biobank	rs10180522
1000 genomes	rs10180522
hgdp	rs10180522
ensembl	rs10180522
geneview	rs10180522
scholar	rs10180522
google	rs10180522
pharmgkb	rs10180522
gwascentral	rs10180522
openSNP	rs10180522
23andMe	rs10180522
SNPshot	rs10180522
SNPdbe	rs10180522
MSV3d	rs10180522
GWAS Ctlg	rs10180522

GMAF

0.2002

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23527680]
Trait	Attention deficit hyperactivity disorder (inattention symptoms)
Title	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Risk Allele	A
P-val	7E-6
Odds Ratio	NR NR