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Variant (rsID / SNP)

rs587776577

WT1

rs587776577 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,413,514. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

WT1Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
11:32413514
Cytoband
11p13
HGVS
NM_024426.6(WT1):c.1447+4C>T
Allele change
Silent

Associated conditions / phenotypes

Frasier syndrome|Nephrotic syndrome, type 4|Familial idiopathic steroid-resistant nephrotic syndrome|Nephrotic range proteinuria|Frasier syndrome|Drash syndrome|Wilms tumor 1|11p partial monosomy syndrome|Wilms tumor 1

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.