Variant (rsID / SNP)

rs121907911

rs121907911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,456,361. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

WT1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:32456361
Cytoband: 11p13
HGVS: NM_024426.6(WT1):c.546C>A (p.Tyr182Ter)
Allele change: Nonsense_Y182X

Associated conditions / phenotypes

Wilms tumor 1

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.