Variant (rsID / SNP)
rs137854379
rs137854379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,124,336. The table records no clinical significance for this variant.
Reference-table entries
TSC2Not classified
- Variant type
- Insertion
- Chromosome / position
- 16:2124336
- Cytoband
- 16p13.3
- HGVS
- NM_000548.5(TSC2):c.2491_2492insAT (p.Thr831fs)
Associated conditions / phenotypes
Tuberous sclerosis syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.