Variant (rsID / SNP)
rs771681406
rs771681406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,456,526. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
WT1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:32456526
- Cytoband
- 11p13
- HGVS
- NM_024426.6(WT1):c.381C>G (p.Pro127=)
- Allele change
- Synonymous_P127P
Associated conditions / phenotypes
Wilms tumor 1|Nephrotic syndrome, type 4|Meacham syndrome|Drash syndrome|Frasier syndrome|Wilms tumor 1|11p partial monosomy syndrome|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.