Variant (rsID / SNP)
rs121907908
rs121907908 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WT1. Location: chromosome 11, position 32,421,571. Clinical significance in the table: Pathogenic.
Reference-table entries
WT1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:32421571
- Cytoband
- 11p13
- HGVS
- NM_024426.6(WT1):c.1036A>G (p.Ser346Gly)
- Allele change
- Missense_S329G
Associated conditions / phenotypes
Mesothelioma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.