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rs6111803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs6111803(G;T)
Make rs6111803(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position18041718
GeneOVOL2
is asnp
is mentioned by
dbSNPrs6111803
ebirs6111803
HLIrs6111803
Exacrs6111803
Varsomers6111803
Maprs6111803
PheGenIrs6111803
hapmaprs6111803
1000 genomesrs6111803
hgdprs6111803
ensemblrs6111803
gopubmedrs6111803
geneviewrs6111803
scholarrs6111803
googlers6111803
pharmgkbrs6111803
gwascentralrs6111803
openSNPrs6111803
23andMers6111803
23andMe allrs6111803
SNP Nexus

SNPshotrs6111803
SNPdbers6111803
MSV3drs6111803
GWAS Ctlgrs6111803
GMAF0.03444
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19574904OA-icon.png] Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval