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rs7323755

From SNPedia

Orientationplus
Stabilizedplus
Make rs7323755(A;A)
Make rs7323755(A;G)
Make rs7323755(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position45326132
is asnp
is mentioned by
dbSNPrs7323755
ebirs7323755
HLIrs7323755
Exacrs7323755
Varsomers7323755
Maprs7323755
PheGenIrs7323755
hapmaprs7323755
1000 genomesrs7323755
hgdprs7323755
ensemblrs7323755
gopubmedrs7323755
geneviewrs7323755
scholarrs7323755
googlers7323755
pharmgkbrs7323755
gwascentralrs7323755
openSNPrs7323755
23andMers7323755
23andMe allrs7323755
SNP Nexus

SNPshotrs7323755
SNPdbers7323755
MSV3drs7323755
GWAS Ctlgrs7323755
GMAF0.06107
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 2E-13
Odds Ratio NR NR