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Variant (rsID / SNP)

rs45517248

TSC2

rs45517248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,125,803. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

TSC2Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
16:2125803
Cytoband
16p13.3
HGVS
NM_000548.5(TSC2):c.2549T>C (p.Leu850Pro)
Allele change
Missense_L850P

Associated conditions / phenotypes

Tuberous sclerosis syndrome|Hereditary cancer-predisposing syndrome|Tuberous sclerosis 2

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.