Variant (rsID / SNP)

rs121907902

rs121907902 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,413,559. 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: 11:32413559
Cytoband: 11p13
HGVS: NM_024426.6(WT1):c.1406A>G (p.Asp469Gly)
Allele change: Missense_D452G

Associated conditions / phenotypes

Drash syndrome|Drash syndrome|Wilms tumor 1|11p partial monosomy syndrome|Frasier syndrome

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.