Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203993

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203993(G;T)
Make rs786203993(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144401308
GeneZEB2
is asnp
is mentioned by
dbSNPrs786203993
ebirs786203993
HLIrs786203993
Exacrs786203993
Varsomers786203993
Maprs786203993
PheGenIrs786203993
hapmaprs786203993
1000 genomesrs786203993
hgdprs786203993
ensemblrs786203993
gopubmedrs786203993
geneviewrs786203993
scholarrs786203993
googlers786203993
pharmgkbrs786203993
gwascentralrs786203993
openSNPrs786203993
23andMers786203993
23andMe allrs786203993
SNP Nexus

SNPshotrs786203993
SNPdbers786203993
MSV3drs786203993
GWAS Ctlgrs786203993
Max Magnitude0
ClinVar
Risk rs786203993(T;T)
Alt rs786203993(T;T)
Reference rs786203993(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ZEB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.145158875C>A
CLNSRC The Children's Hospital of Philadelphia
CLNACC RCV000167556.1,