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Variant (rsID / SNP)

rs185223937

ZEB2

rs185223937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZEB2. Location: chromosome 2, position 145,155,988. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZEB2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:145155988
Cytoband
2q22.3
HGVS
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=)
Allele change
Synonymous_P898P

Associated conditions / phenotypes

History of neurodevelopmental disorder|Mowat-Wilson syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.