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rs11618212

From SNPedia

Orientationplus
Stabilizedplus
Make rs11618212(A;A)
Make rs11618212(A;G)
Make rs11618212(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position105444463
is asnp
is mentioned by
dbSNPrs11618212
ebirs11618212
HLIrs11618212
Exacrs11618212
Varsomers11618212
Maprs11618212
PheGenIrs11618212
hapmaprs11618212
1000 genomesrs11618212
hgdprs11618212
ensemblrs11618212
gopubmedrs11618212
geneviewrs11618212
scholarrs11618212
googlers11618212
pharmgkbrs11618212
gwascentralrs11618212
openSNPrs11618212
23andMers11618212
23andMe allrs11618212
SNP Nexus

SNPshotrs11618212
SNPdbers11618212
MSV3drs11618212
GWAS Ctlgrs11618212
GMAF0.152
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23049088]
Trait Myopia (pathological)
Title A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val 5E-12
Odds Ratio NR NR