Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs527655625

WT1

rs527655625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,421,548. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

WT1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:32421548
Cytoband
11p13
HGVS
NM_024426.6(WT1):c.1059C>T (p.Ile353_Leu354=)
Allele change
Synonymous_I336I

Associated conditions / phenotypes

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.