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Variant (rsID / SNP)

rs202113269

DNAAF1

rs202113269 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAAF1. Location: chromosome 16, position 84,199,569. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAAF1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:84199569
Cytoband
16q24.1
HGVS
NM_178452.6(DNAAF1):c.1030+14C>T
Allele change
Silent

Associated conditions / phenotypes

Primary ciliary dyskinesia 13|Primary ciliary dyskinesia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.