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rs9607469

From SNPedia

Orientationplus
Stabilizedplus
Make rs9607469(A;A)
Make rs9607469(A;G)
Make rs9607469(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37523260
is asnp
is mentioned by
dbSNPrs9607469
ebirs9607469
HLIrs9607469
Exacrs9607469
Varsomers9607469
Maprs9607469
PheGenIrs9607469
hapmaprs9607469
1000 genomesrs9607469
hgdprs9607469
ensemblrs9607469
gopubmedrs9607469
geneviewrs9607469
scholarrs9607469
googlers9607469
pharmgkbrs9607469
gwascentralrs9607469
openSNPrs9607469
23andMers9607469
23andMe allrs9607469
SNP Nexus

SNPshotrs9607469
SNPdbers9607469
MSV3drs9607469
GWAS Ctlgrs9607469
GMAF0.1662
Max Magnitude
? (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