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rs7837791

From SNPedia

Orientationplus
Stabilizedplus
Make rs7837791(G;G)
Make rs7837791(G;T)
Make rs7837791(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position59266527
is asnp
is mentioned by
dbSNPrs7837791
ebirs7837791
HLIrs7837791
Exacrs7837791
Varsomers7837791
Maprs7837791
PheGenIrs7837791
hapmaprs7837791
1000 genomesrs7837791
hgdprs7837791
ensemblrs7837791
gopubmedrs7837791
geneviewrs7837791
scholarrs7837791
googlers7837791
pharmgkbrs7837791
gwascentralrs7837791
openSNPrs7837791
23andMers7837791
23andMe allrs7837791
SNP Nexus

SNPshotrs7837791
SNPdbers7837791
MSV3drs7837791
GWAS Ctlgrs7837791
GMAF0.4568
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele T
P-val 4E-12
Odds Ratio .11 [0.077-0.135] unit increase


[PMID 25628894OA-icon.png] Evaluation of four genetic variants in han chinese subjects with high myopia