Variant (rsID / SNP)

rs369622877

rs369622877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZEB2. Location: chromosome 2, position 145,182,371. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZEB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:145182371
Cytoband: 2q22.3
HGVS: NM_014795.4(ZEB2):c.395A>G (p.Asn132Ser)
Allele change: Silent

Associated conditions / phenotypes

Mowat-Wilson syndrome

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.