rs490592

Orientation

minus

Stabilized

minus

Make rs490592(G;G)

Make rs490592(G;T)

Make rs490592(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

116427650

Gene	LOC107987166

is a	snp
is	mentioned by
dbSNP	rs490592
dbSNP (classic)	rs490592
ClinGen	rs490592
ebi	rs490592
HLI	rs490592
Exac	rs490592
Gnomad	rs490592
Varsome	rs490592
LitVar	rs490592
Map	rs490592
PheGenI	rs490592
Biobank	rs490592
1000 genomes	rs490592
hgdp	rs490592
ensembl	rs490592
geneview	rs490592
scholar	rs490592
google	rs490592
pharmgkb	rs490592
gwascentral	rs490592
openSNP	rs490592
23andMe	rs490592
SNPshot	rs490592
SNPdbe	rs490592
MSV3d	rs490592
GWAS Ctlg	rs490592

GMAF

0.1791

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

GWAS snp
PMID	[PMID 20171287]
Trait	Brain structure
Title	Voxelwise Genome-Wide Association Study (vGWAS).
Risk Allele
P-val	0.000001
Odds Ratio	None None