Variant (rsID / SNP)

rs9944927

rs9944927 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTNA. Location: chromosome 18, position 32,470,291. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DTNABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:32470291
Cytoband: 18q12.1
HGVS: NM_001386795.1(DTNA):c.*2593G>A
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.