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rs786203991

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203991(-;-)
Make rs786203991(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144389552
GeneZEB2
is asnp
is mentioned by
dbSNPrs786203991
ebirs786203991
HLIrs786203991
Exacrs786203991
Varsomers786203991
Maprs786203991
PheGenIrs786203991
hapmaprs786203991
1000 genomesrs786203991
hgdprs786203991
ensemblrs786203991
gopubmedrs786203991
geneviewrs786203991
scholarrs786203991
googlers786203991
pharmgkbrs786203991
gwascentralrs786203991
openSNPrs786203991
23andMers786203991
23andMe allrs786203991
SNP Nexus

SNPshotrs786203991
SNPdbers786203991
MSV3drs786203991
GWAS Ctlgrs786203991
Max Magnitude0
ClinVar
Risk rs786203991(;)
Alt rs786203991(;)
Reference rs786203991(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ZEB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.145147119delC
CLNSRC The Children's Hospital of Philadelphia
CLNACC RCV000167553.1,