Variant (rsID / SNP)
rs754532627
rs754532627 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZEB2. Location: chromosome 2, position 145,155,864. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
ZEB2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:145155864
- Cytoband
- 2q22.3
- HGVS
- NM_014795.4(ZEB2):c.2886+4A>C
- Allele change
- Silent
Associated conditions / phenotypes
Mowat-Wilson syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.