Variant (rsID / SNP)
rs555140661
rs555140661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,456,784. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
WT1Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:32456784
- Cytoband
- 11p13
- HGVS
- NM_024426.6(WT1):c.123G>C (p.Pro41=)
- Allele change
- Synonymous_P41P
Associated conditions / phenotypes
Meacham syndrome|Nephrotic syndrome, type 4|Wilms tumor 1|Wilms tumor 1|11p partial monosomy syndrome|Drash syndrome|Frasier 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.