Variant (rsID / SNP)
rs1064793646
rs1064793646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,136,763. Clinical significance in the table: Pathogenic.
Reference-table entries
TSC2Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 16:2136763
- Cytoband
- 16p13.3
- HGVS
- NM_000548.5(TSC2):c.4881del (p.Lys1628fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.