Variant (rsID / SNP)

rs28941777

rs28941777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,413,599. Clinical significance in the table: Pathogenic.

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Reference-table entries

WT1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:32413599
Cytoband: 11p13
HGVS: NM_024426.6(WT1):c.1366T>C (p.Phe456Leu)
Allele change: Missense_F439L

Associated conditions / phenotypes

Nephrotic syndrome, type 4

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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