Variant (rsID / SNP)

rs61739410

rs61739410 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTNBP1. Location: chromosome 6, position 15,533,469. Clinical significance in the table: Benign.

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Reference-table entries

DTNBP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:15533469
Cytoband: 6p22.3
HGVS: NM_032122.5(DTNBP1):c.667+2C>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.