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rs17826255

From SNPedia

Orientationplus
Stabilizedplus
Make rs17826255(C;C)
Make rs17826255(C;T)
Make rs17826255(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31006498
GeneZNF41
is asnp
is mentioned by
dbSNPrs17826255
ebirs17826255
HLIrs17826255
Exacrs17826255
Varsomers17826255
Maprs17826255
PheGenIrs17826255
hapmaprs17826255
1000 genomesrs17826255
hgdprs17826255
ensemblrs17826255
gopubmedrs17826255
geneviewrs17826255
scholarrs17826255
googlers17826255
pharmgkbrs17826255
gwascentralrs17826255
openSNPrs17826255
23andMers17826255
23andMe allrs17826255
SNP Nexus

SNPshotrs17826255
SNPdbers17826255
MSV3drs17826255
GWAS Ctlgrs17826255
GMAF0.07208
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 8E-9
Odds Ratio NR NR