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rs7823896

From SNPedia

Orientationplus
Stabilizedplus
Make rs7823896(C;C)
Make rs7823896(C;T)
Make rs7823896(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position109205037
is asnp
is mentioned by
dbSNPrs7823896
ebirs7823896
HLIrs7823896
Exacrs7823896
Varsomers7823896
Maprs7823896
PheGenIrs7823896
hapmaprs7823896
1000 genomesrs7823896
hgdprs7823896
ensemblrs7823896
gopubmedrs7823896
geneviewrs7823896
scholarrs7823896
googlers7823896
pharmgkbrs7823896
gwascentralrs7823896
openSNPrs7823896
23andMers7823896
23andMe allrs7823896
SNP Nexus

SNPshotrs7823896
SNPdbers7823896
MSV3drs7823896
GWAS Ctlgrs7823896
GMAF0.2433
Max Magnitude
? (C;C) (C;T) (T;T) 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 3E-6
Odds Ratio NR NR