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

rs17648524

From SNPedia

Orientationplus
Stabilizedplus
Make rs17648524(C;C)
Make rs17648524(C;G)
Make rs17648524(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position7409682
GeneRBFOX1
is asnp
is mentioned by
dbSNPrs17648524
ebirs17648524
HLIrs17648524
Exacrs17648524
Varsomers17648524
Maprs17648524
PheGenIrs17648524
hapmaprs17648524
1000 genomesrs17648524
hgdprs17648524
ensemblrs17648524
gopubmedrs17648524
geneviewrs17648524
scholarrs17648524
googlers17648524
pharmgkbrs17648524
gwascentralrs17648524
openSNPrs17648524
23andMers17648524
23andMe allrs17648524
SNP Nexus

SNPshotrs17648524
SNPdbers17648524
MSV3drs17648524
GWAS Ctlgrs17648524
GMAF0.2268
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 6E-10
Odds Ratio .12 [0.081-0.155] unit decrease