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rs248471

From SNPedia

Orientationplus
Stabilizedplus
Make rs248471(A;A)
Make rs248471(A;G)
Make rs248471(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position141809602
is asnp
is mentioned by
dbSNPrs248471
ebirs248471
HLIrs248471
Exacrs248471
Varsomers248471
Maprs248471
PheGenIrs248471
hapmaprs248471
1000 genomesrs248471
hgdprs248471
ensemblrs248471
gopubmedrs248471
geneviewrs248471
scholarrs248471
googlers248471
pharmgkbrs248471
gwascentralrs248471
openSNPrs248471
23andMers248471
23andMe allrs248471
SNP Nexus

SNPshotrs248471
SNPdbers248471
MSV3drs248471
GWAS Ctlgrs248471
GMAF0.4261
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23406873]
Trait Myopia (pathological)
Title A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.
Risk Allele G
P-val 2E-6
Odds Ratio 1.19 [1.11-1.28]