Variant (rsID / SNP)

rs146442289

rs146442289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAAF3. Location: chromosome 19, position 55,672,156. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAAF3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:55672156
Cytoband: 19q13.42
HGVS: NM_001256715.2(DNAAF3):c.913-13C>T
Allele change: Silent

Associated conditions / phenotypes

Primary ciliary dyskinesia

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.