Variant (rsID / SNP)

rs6711223

rs6711223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZEB2. Location: chromosome 2, position 145,157,824. Clinical significance in the table: Benign.

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Reference-table entries

ZEB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:145157824
Cytoband: 2q22.3
HGVS: NM_014795.4(ZEB2):c.930C>T (p.Tyr310=)
Allele change: Synonymous_Y286Y

Associated conditions / phenotypes

Mowat-Wilson syndrome|History of neurodevelopmental disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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