Variant (rsID / SNP)

rs57809907

rs57809907 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAAF4. Location: chromosome 15, position 55,722,882. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAAF4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:55722882
Cytoband: 15q21.3
HGVS: NM_130810.4(DNAAF4):c.1249G>T (p.Glu417Ter)
Allele change: Silent

Associated conditions / phenotypes

Dyslexia, susceptibility to, 1|Primary ciliary dyskinesia 25

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.