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rs1302019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
Make rs1302019(A;G)
Make rs1302019(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position147650438
is asnp
is mentioned by
dbSNPrs1302019
ebirs1302019
HLIrs1302019
Exacrs1302019
Varsomers1302019
Maprs1302019
PheGenIrs1302019
hapmaprs1302019
1000 genomesrs1302019
hgdprs1302019
ensemblrs1302019
gopubmedrs1302019
geneviewrs1302019
scholarrs1302019
googlers1302019
pharmgkbrs1302019
gwascentralrs1302019
openSNPrs1302019
23andMers1302019
23andMe allrs1302019
SNP Nexus

SNPshotrs1302019
SNPdbers1302019
MSV3drs1302019
GWAS Ctlgrs1302019
GMAF0.0528
Max Magnitude0
? (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-23
Odds Ratio NR NR