Variant (rsID / SNP)

rs352810

rs352810 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUSC3. Location: chromosome 8, position 15,622,519. Clinical significance in the table: Benign.

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Reference-table entries

TUSC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:15622519
Cytoband: 8p22
HGVS: NM_006765.4(TUSC3):c.*854T>C
Allele change: Silent

Associated conditions / phenotypes

Congenital disorder of glycosylation

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.