Have questions? Visit https://www.reddit.com/r/SNPedia

rs872863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs872863(C;T)
Make rs872863(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position123392075
GeneDENND1A
is asnp
is mentioned by
dbSNPrs872863
ebirs872863
HLIrs872863
Exacrs872863
Varsomers872863
Maprs872863
PheGenIrs872863
hapmaprs872863
1000 genomesrs872863
hgdprs872863
ensemblrs872863
gopubmedrs872863
geneviewrs872863
scholarrs872863
googlers872863
pharmgkbrs872863
gwascentralrs872863
openSNPrs872863
23andMers872863
23andMe allrs872863
SNP Nexus

SNPshotrs872863
SNPdbers872863
MSV3drs872863
GWAS Ctlgrs872863
GMAF0.0854
Max Magnitude0
? (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 2E-11
Odds Ratio NR NR


[PMID 20018028OA-icon.png] Armitage's trend test for genome-wide association analysis: one-sided or two-sided?