Variant (rsID / SNP)

rs1349302999

rs1349302999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,450,128. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

WT1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:32450128
Cytoband: 11p13
HGVS: NM_024426.6(WT1):c.699C>A (p.Tyr233Ter)
Allele change: Nonsense_Y233X

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.