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

rs6472235

From SNPedia

Orientationplus
Stabilizedplus
Make rs6472235(G;G)
Make rs6472235(G;T)
Make rs6472235(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position65909795
is asnp
is mentioned by
dbSNPrs6472235
ebirs6472235
HLIrs6472235
Exacrs6472235
Varsomers6472235
Maprs6472235
PheGenIrs6472235
hapmaprs6472235
1000 genomesrs6472235
hgdprs6472235
ensemblrs6472235
gopubmedrs6472235
geneviewrs6472235
scholarrs6472235
googlers6472235
pharmgkbrs6472235
gwascentralrs6472235
openSNPrs6472235
23andMers6472235
23andMe allrs6472235
SNP Nexus

SNPshotrs6472235
SNPdbers6472235
MSV3drs6472235
GWAS Ctlgrs6472235
GMAF0.3967
Max Magnitude
? (G;G) (G;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 1E-7
Odds Ratio NR NR