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Variant (rsID / SNP)

rs397515169

TSC2

rs397515169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,131,594. The table records no clinical significance for this variant.

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Reference-table entries

TSC2Not classified
Variant type
single nucleotide variant
Chromosome / position
16:2131594
Cytoband
16p13.3
HGVS
NM_000548.5(TSC2):c.3611-2A>T
Allele change
Silent

Associated conditions / phenotypes

Tuberous sclerosis syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.