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rs4737395

From SNPedia

Orientationplus
Stabilizedplus
Make rs4737395(A;A)
Make rs4737395(A;G)
Make rs4737395(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position55686989
is asnp
is mentioned by
dbSNPrs4737395
ebirs4737395
HLIrs4737395
Exacrs4737395
Varsomers4737395
Maprs4737395
PheGenIrs4737395
hapmaprs4737395
1000 genomesrs4737395
hgdprs4737395
ensemblrs4737395
gopubmedrs4737395
geneviewrs4737395
scholarrs4737395
googlers4737395
pharmgkbrs4737395
gwascentralrs4737395
openSNPrs4737395
23andMers4737395
23andMe allrs4737395
SNP Nexus

SNPshotrs4737395
SNPdbers4737395
MSV3drs4737395
GWAS Ctlgrs4737395
GMAF0.1263
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-9
Odds Ratio NR NR