Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057518956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518956(C;T)
Make rs1057518956(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position31520308
GeneZEB1
is asnp
is mentioned by
dbSNPrs1057518956
dbSNP (old)rs1057518956
ClinGenrs1057518956
ebirs1057518956
HLIrs1057518956
Exacrs1057518956
Gnomadrs1057518956
Varsomers1057518956
Maprs1057518956
PheGenIrs1057518956
Biobankrs1057518956
1000 genomesrs1057518956
hgdprs1057518956
ensemblrs1057518956
gopubmedrs1057518956
geneviewrs1057518956
scholarrs1057518956
googlers1057518956
pharmgkbrs1057518956
gwascentralrs1057518956
openSNPrs1057518956
23andMers1057518956
23andMe allrs1057518956
SNPshotrs1057518956
SNPdbers1057518956
MSV3drs1057518956
GWAS Ctlgrs1057518956
Max Magnitude0
ClinVar
Risk rs1057518956(T;T)
Alt rs1057518956(T;T)
Reference Rs1057518956(C;C)
Significance Pathogenic
Disease Glaucoma Polymorphous posterior corneal dystrophy Visual loss
Variation info
Gene ZEB1
CLNDBN Glaucoma Polymorphous posterior corneal dystrophy Visual loss
Reversed 0
HGVS NC_000010.10:g.31809236C>T
CLNSRC
CLNACC RCV000415113.1,