Variant (rsID / SNP)

rs201835391

rs201835391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,126,510. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TSC2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:2126510
Cytoband: 16p13.3
HGVS: NM_000548.5(TSC2):c.2761C>G (p.Leu921Val)
Allele change: Missense_L921V

Associated conditions / phenotypes

Tuberous sclerosis 2|History of neurodevelopmental disorder|Hereditary cancer-predisposing 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.