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rs4838605

From SNPedia

Orientationplus
Stabilizedplus
Make rs4838605(C;C)
Make rs4838605(C;T)
Make rs4838605(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position48491914
GeneARHGAP22
is asnp
is mentioned by
dbSNPrs4838605
ebirs4838605
HLIrs4838605
Exacrs4838605
Varsomers4838605
Maprs4838605
PheGenIrs4838605
hapmaprs4838605
1000 genomesrs4838605
hgdprs4838605
ensemblrs4838605
gopubmedrs4838605
geneviewrs4838605
scholarrs4838605
googlers4838605
pharmgkbrs4838605
gwascentralrs4838605
openSNPrs4838605
23andMers4838605
23andMe allrs4838605
SNP Nexus

SNPshotrs4838605
SNPdbers4838605
MSV3drs4838605
GWAS Ctlgrs4838605
GMAF0.4766
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21310492]
Trait
Title Genome-wide Association Study of Diabetic Retinopathy in a Taiwanese Population
Risk Allele C
P-val 2E-9
Odds Ratio None None