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rs786203992

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203992(-;-)
Make rs786203992(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144398822
GeneZEB2
is asnp
is mentioned by
dbSNPrs786203992
ebirs786203992
HLIrs786203992
Exacrs786203992
Varsomers786203992
Maprs786203992
PheGenIrs786203992
hapmaprs786203992
1000 genomesrs786203992
hgdprs786203992
ensemblrs786203992
gopubmedrs786203992
geneviewrs786203992
scholarrs786203992
googlers786203992
pharmgkbrs786203992
gwascentralrs786203992
openSNPrs786203992
23andMers786203992
23andMe allrs786203992
SNP Nexus

SNPshotrs786203992
SNPdbers786203992
MSV3drs786203992
GWAS Ctlgrs786203992
Max Magnitude0
ClinVar
Risk rs786203992(;)
Alt rs786203992(;)
Reference rs786203992(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ZEB2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.145156389delA
CLNSRC The Children's Hospital of Philadelphia
CLNACC RCV000167555.1,