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rs10500355

From SNPedia

Orientationplus
Stabilizedplus
Make rs10500355(A;A)
Make rs10500355(A;T)
Make rs10500355(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position7409346
GeneRBFOX1
is asnp
is mentioned by
dbSNPrs10500355
ebirs10500355
HLIrs10500355
Exacrs10500355
Varsomers10500355
Maprs10500355
PheGenIrs10500355
hapmaprs10500355
1000 genomesrs10500355
hgdprs10500355
ensemblrs10500355
gopubmedrs10500355
geneviewrs10500355
scholarrs10500355
googlers10500355
pharmgkbrs10500355
gwascentralrs10500355
openSNPrs10500355
23andMers10500355
23andMe allrs10500355
SNP Nexus

SNPshotrs10500355
SNPdbers10500355
MSV3drs10500355
GWAS Ctlgrs10500355
GMAF0.2241
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 23474815OA-icon.png] Meta-Analysis of Genome-wide Association Studies in 5 cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error