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rs7077335

From SNPedia

Orientationplus
Stabilizedplus
Make rs7077335(A;A)
Make rs7077335(A;C)
Make rs7077335(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position6273831
is asnp
is mentioned by
dbSNPrs7077335
ebirs7077335
HLIrs7077335
Exacrs7077335
Varsomers7077335
Maprs7077335
PheGenIrs7077335
hapmaprs7077335
1000 genomesrs7077335
hgdprs7077335
ensemblrs7077335
gopubmedrs7077335
geneviewrs7077335
scholarrs7077335
googlers7077335
pharmgkbrs7077335
gwascentralrs7077335
openSNPrs7077335
23andMers7077335
23andMe allrs7077335
SNP Nexus

SNPshotrs7077335
SNPdbers7077335
MSV3drs7077335
GWAS Ctlgrs7077335
GMAF0.1878
Max Magnitude
? (A;A) (A;C) (C;C) 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-12
Odds Ratio NR NR