Variant (rsID / SNP)

rs1057518945

rs1057518945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,797,211. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TSC1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 9:135797211
Cytoband: 9q34.13
HGVS: NM_000368.5(TSC1):c.658del (p.Val220fs)

Associated conditions / phenotypes

Cortical tubers|Adenoma sebaceum

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.