Variant (rsID / SNP)

rs587781774

rs587781774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,129,420. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TSC2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:2129420
Cytoband: 16p13.3
HGVS: NM_000548.5(TSC2):c.3275C>T (p.Pro1092Leu)
Allele change: Missense_P1049L

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Tuberous sclerosis 2

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.