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rs118020901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 4 Corneal dystrophy, fuchs endothelial, 6
Make rs118020901(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position31521854
GeneZEB1
is asnp
is mentioned by
dbSNPrs118020901
ebirs118020901
HLIrs118020901
Exacrs118020901
Varsomers118020901
Maprs118020901
PheGenIrs118020901
hapmaprs118020901
1000 genomesrs118020901
hgdprs118020901
ensemblrs118020901
gopubmedrs118020901
geneviewrs118020901
scholarrs118020901
googlers118020901
pharmgkbrs118020901
gwascentralrs118020901
openSNPrs118020901
23andMers118020901
23andMe allrs118020901
SNP Nexus

SNPshotrs118020901
SNPdbers118020901
MSV3drs118020901
GWAS Ctlgrs118020901
GMAF0.00551
Max Magnitude4
ClinVar
Risk rs118020901(C;C)
Alt rs118020901(C;C)
Reference rs118020901(A;A)
Significance Pathogenic
Disease Corneal dystrophy
Variation info
Gene ZEB1
CLNDBN Corneal dystrophy, Fuchs endothelial, 6
Reversed 0
HGVS NC_000010.10:g.31810782A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013469.17,