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rs1060499770

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GGTGGAG;GGTGGAG) 0 common in clinvar
Make rs1060499770(-;-)
Make rs1060499770(-;GGTGGAG)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position144429823
GeneZEB2
is asnp
is mentioned by
dbSNPrs1060499770
dbSNP (old)rs1060499770
ClinGenrs1060499770
ebirs1060499770
HLIrs1060499770
Exacrs1060499770
Gnomadrs1060499770
Varsomers1060499770
Maprs1060499770
PheGenIrs1060499770
Biobankrs1060499770
1000 genomesrs1060499770
hgdprs1060499770
ensemblrs1060499770
gopubmedrs1060499770
geneviewrs1060499770
scholarrs1060499770
googlers1060499770
pharmgkbrs1060499770
gwascentralrs1060499770
openSNPrs1060499770
23andMers1060499770
23andMe allrs1060499770
SNPshotrs1060499770
SNPdbers1060499770
MSV3drs1060499770
GWAS Ctlgrs1060499770
Max Magnitude0
ClinVar
Risk rs1060499770(-;-)
Alt rs1060499770(-;-)
Reference Rs1060499770(GGTGGAG;GGTGGAG)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ZEB2
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000002.11:g.145187390_145187396delCTCCACC
CLNSRC
CLNACC RCV000454268.1,