Have questions? Visit https://www.reddit.com/r/SNPedia

rs11601239

From SNPedia

Orientationplus
Stabilizedplus
Make rs11601239(C;C)
Make rs11601239(C;G)
Make rs11601239(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position105685872
GeneGRIA4
is asnp
is mentioned by
dbSNPrs11601239
ebirs11601239
HLIrs11601239
Exacrs11601239
Varsomers11601239
Maprs11601239
PheGenIrs11601239
hapmaprs11601239
1000 genomesrs11601239
hgdprs11601239
ensemblrs11601239
gopubmedrs11601239
geneviewrs11601239
scholarrs11601239
googlers11601239
pharmgkbrs11601239
gwascentralrs11601239
openSNPrs11601239
23andMers11601239
23andMe allrs11601239
SNP Nexus

SNPshotrs11601239
SNPdbers11601239
MSV3drs11601239
GWAS Ctlgrs11601239
GMAF0.449
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele C
P-val 6E-9
Odds Ratio .10 [0.064-0.126] unit decrease