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rs1944866

From SNPedia

Orientationplus
Stabilizedplus
Make rs1944866(C;C)
Make rs1944866(C;T)
Make rs1944866(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position134612572
is asnp
is mentioned by
dbSNPrs1944866
ebirs1944866
HLIrs1944866
Exacrs1944866
Varsomers1944866
Maprs1944866
PheGenIrs1944866
hapmaprs1944866
1000 genomesrs1944866
hgdprs1944866
ensemblrs1944866
gopubmedrs1944866
geneviewrs1944866
scholarrs1944866
googlers1944866
pharmgkbrs1944866
gwascentralrs1944866
openSNPrs1944866
23andMers1944866
23andMe allrs1944866
SNP Nexus

SNPshotrs1944866
SNPdbers1944866
MSV3drs1944866
GWAS Ctlgrs1944866
GMAF0.2144
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 2E-6
Odds Ratio NR NR