rs9607469

Orientation

plus

Stabilized

plus

Make rs9607469(A;A)

Make rs9607469(A;G)

Make rs9607469(G;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

37523260

is a	snp
is	mentioned by
dbSNP	rs9607469
dbSNP (classic)	rs9607469
ClinGen	rs9607469
ebi	rs9607469
HLI	rs9607469
Exac	rs9607469
Gnomad	rs9607469
Varsome	rs9607469
LitVar	rs9607469
Map	rs9607469
PheGenI	rs9607469
Biobank	rs9607469
1000 genomes	rs9607469
hgdp	rs9607469
ensembl	rs9607469
geneview	rs9607469
scholar	rs9607469
google	rs9607469
pharmgkb	rs9607469
gwascentral	rs9607469
openSNP	rs9607469
23andMe	rs9607469
SNPshot	rs9607469
SNPdbe	rs9607469
MSV3d	rs9607469
GWAS Ctlg	rs9607469

GMAF

0.1662

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21307088]
Trait
Title	Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
Risk Allele	A
P-val	3E-12
Odds Ratio	0.0510 [0.04-0.06] mm2 increase