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Variant (rsID / SNP)

rs377598226

TSC1

rs377598226 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,786,058. 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
9:135786058
Cytoband
9q34.13
HGVS
NM_000368.5(TSC1):c.1163T>C (p.Leu388Pro)
Allele change
Missense_L337P

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Tuberous sclerosis 1

Public references

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