Variant (rsID / SNP)

rs886041758

rs886041758 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,108,829. Clinical significance in the table: Pathogenic.

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Reference-table entries

TSC2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:2108829
Cytoband: 16p13.3
HGVS: NM_000548.5(TSC2):c.930T>A (p.Tyr310Ter)
Allele change: Nonsense_Y310X

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.