Variant (rsID / SNP)
rs118203682
rs118203682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,778,027. Clinical significance in the table: Pathogenic.
Reference-table entries
TSC1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:135778027
- Cytoband
- 9q34.13
- HGVS
- NM_000368.5(TSC1):c.2356C>T (p.Arg786Ter)
- Allele change
- Nonsense_R735X
Associated conditions / phenotypes
Tuberous sclerosis syndrome|Tuberous sclerosis 1|Seizure|Hamartoma|Cardiac rhabdomyoma|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.