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rs1057510

From SNPedia

Orientationplus
Stabilizedplus
Make rs1057510(A;A)
Make rs1057510(A;G)
Make rs1057510(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6574121
GeneCHD4
is asnp
is mentioned by
dbSNPrs1057510
ebirs1057510
HLIrs1057510
Exacrs1057510
Varsomers1057510
Maprs1057510
PheGenIrs1057510
hapmaprs1057510
1000 genomesrs1057510
hgdprs1057510
ensemblrs1057510
gopubmedrs1057510
geneviewrs1057510
scholarrs1057510
googlers1057510
pharmgkbrs1057510
gwascentralrs1057510
openSNPrs1057510
23andMers1057510
23andMe allrs1057510
SNP Nexus

SNPshotrs1057510
SNPdbers1057510
MSV3drs1057510
GWAS Ctlgrs1057510
GMAF0.3067
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 6E-6
Odds Ratio NR NR