Variant (rsID / SNP)

rs118203402

rs118203402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,797,300. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TSC1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:135797300
Cytoband: 9q34.13
HGVS: NM_000368.5(TSC1):c.569G>C (p.Arg190Pro)
Allele change: Missense_R139P

Associated conditions / phenotypes

Tuberous sclerosis syndrome

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.