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rs6841898

From SNPedia

Orientationplus
Stabilizedplus
Make rs6841898(C;C)
Make rs6841898(C;T)
Make rs6841898(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position24576474
GeneDHX15
is asnp
is mentioned by
dbSNPrs6841898
ebirs6841898
HLIrs6841898
Exacrs6841898
Varsomers6841898
Maprs6841898
PheGenIrs6841898
hapmaprs6841898
1000 genomesrs6841898
hgdprs6841898
ensemblrs6841898
gopubmedrs6841898
geneviewrs6841898
scholarrs6841898
googlers6841898
pharmgkbrs6841898
gwascentralrs6841898
openSNPrs6841898
23andMers6841898
23andMe allrs6841898
SNP Nexus

SNPshotrs6841898
SNPdbers6841898
MSV3drs6841898
GWAS Ctlgrs6841898
GMAF0.05877
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-26
Odds Ratio NR NR