Variant (rsID / SNP)

rs118203614

rs118203614 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC1. Location: chromosome 9, position 135,779,842. The table records no clinical significance for this variant.

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Reference-table entries

TSC1Not classified

Variant type: single nucleotide variant
Chromosome / position: 9:135779842
Cytoband: 9q34.13
HGVS: NM_000368.5(TSC1):c.1998-1G>A
Allele change: Silent

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.