Variant (rsID / SNP)
rs16754
rs16754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,417,945. Clinical significance in the table: Benign.
Reference-table entries
WT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:32417945
- Cytoband
- 11p13
- HGVS
- NM_024426.6(WT1):c.1122A>G (p.Arg374_Arg375=)
- Allele change
- Synonymous_R357R
Associated conditions / phenotypes
Nephrotic syndrome, type 4|Meacham syndrome|Wilms tumor 1|Drash syndrome|Frasier syndrome|Nephrotic syndrome, type 4|Wilms tumor 1|Drash syndrome|Frasier syndrome|Wilms tumor 1|11p partial monosomy syndrome|Drash syndrome|Frasier syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.