Variant (rsID / SNP)

rs146546977

rs146546977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTNBP1. Location: chromosome 6, position 15,615,499. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DTNBP1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:15615499
Cytoband: 6p22.3
HGVS: NM_032122.5(DTNBP1):c.487A>C (p.Arg163=)
Allele change: Synonymous_R163R

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.