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Variant (rsID / SNP)

rs199620268

TSC1

rs199620268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,800,991. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TSC1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:135800991
Cytoband
9q34.13
HGVS
NM_000368.5(TSC1):c.346T>G (p.Leu116Val)
Allele change
Silent

Associated conditions / phenotypes

Autism spectrum disorder|Tuberous sclerosis syndrome|Hereditary cancer-predisposing syndrome|Isolated focal cortical dysplasia type II|Tuberous sclerosis 1

Public references

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