Variant (rsID / SNP)

rs16876571

rs16876571 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTNBP1. Location: chromosome 6, position 15,524,679. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DTNBP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:15524679
Cytoband: 6p22.3
HGVS: NM_032122.5(DTNBP1):c.811+78C>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.