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Variant (rsID / SNP)

rs146434058

DNAI1

rs146434058 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAI1. Location: chromosome 9, position 34,517,393. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DNAI1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
9:34517393
Cytoband
9p13.3
HGVS
NM_012144.4(DNAI1):c.1929C>A (p.Ile643=)
Allele change
Synonymous_I647I

Associated conditions / phenotypes

Primary ciliary dyskinesia|Kartagener syndrome

Public references

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