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

rs1045529

From SNPedia

Orientationplus
Stabilizedplus
Make rs1045529(C;C)
Make rs1045529(C;T)
Make rs1045529(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position9032588
GeneERI1
is asnp
is mentioned by
dbSNPrs1045529
ebirs1045529
HLIrs1045529
Exacrs1045529
Varsomers1045529
Maprs1045529
PheGenIrs1045529
hapmaprs1045529
1000 genomesrs1045529
hgdprs1045529
ensemblrs1045529
gopubmedrs1045529
geneviewrs1045529
scholarrs1045529
googlers1045529
pharmgkbrs1045529
gwascentralrs1045529
openSNPrs1045529
23andMers1045529
23andMe allrs1045529
SNP Nexus

SNPshotrs1045529
SNPdbers1045529
MSV3drs1045529
GWAS Ctlgrs1045529
GMAF0.4536
Max Magnitude
? (C;C) (C;T) (T;T) 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 3E-6
Odds Ratio NR NR