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rs10490775

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10490775(A;A)
Make rs10490775(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position62051050
GenePTPRG
is asnp
is mentioned by
dbSNPrs10490775
ebirs10490775
HLIrs10490775
Exacrs10490775
Varsomers10490775
Maprs10490775
PheGenIrs10490775
hapmaprs10490775
1000 genomesrs10490775
hgdprs10490775
ensemblrs10490775
gopubmedrs10490775
geneviewrs10490775
scholarrs10490775
googlers10490775
pharmgkbrs10490775
gwascentralrs10490775
openSNPrs10490775
23andMers10490775
23andMe allrs10490775
SNP Nexus

SNPshotrs10490775
SNPdbers10490775
MSV3drs10490775
GWAS Ctlgrs10490775
GMAF0.0854
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20825314]
Trait
Title E2-2 protein and Fuchs's corneal dystrophy
Risk Allele A
P-val 0.000001
Odds Ratio 2.30 [1.64-3.22]