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rs6711223

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6711223(A;A)
Make rs6711223(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144400257
GeneZEB2
is asnp
is mentioned by
dbSNPrs6711223
ebirs6711223
HLIrs6711223
Exacrs6711223
Varsomers6711223
Maprs6711223
PheGenIrs6711223
hapmaprs6711223
1000 genomesrs6711223
hgdprs6711223
ensemblrs6711223
gopubmedrs6711223
geneviewrs6711223
scholarrs6711223
googlers6711223
pharmgkbrs6711223
gwascentralrs6711223
openSNPrs6711223
23andMers6711223
23andMe allrs6711223
SNP Nexus

SNPshotrs6711223
SNPdbers6711223
MSV3drs6711223
GWAS Ctlgrs6711223
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs6711223(A,T;A,T)
Alt rs6711223(A,T;A,T)
Reference rs6711223(G;G)
Significance Pathogenic
Disease not specified Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN not specified Mowat-Wilson syndrome
Reversed 0
HGVS NC_000002.11:g.145157824G>A; NC_000002.11:g.145157824G>T
CLNSRC HGMD
CLNACC RCV000081677.6, RCV000232228.1, RCV000154157.3,