Variant (rsID / SNP)

rs587778004

rs587778004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2, NTHL1. Location: chromosome 16, position 2,098,067. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TSC2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 16:2098067
Cytoband: 16p13.3
HGVS: NM_000548.5(TSC2):c.-30+1G>T
Allele change: Silent

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.