Variant (rsID / SNP)

rs59499600

rs59499600 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAI2. Location: chromosome 17, position 72,301,501. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAI2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:72301501
Cytoband: 17q25.1
HGVS: NM_023036.6(DNAI2):c.1131G>A (p.Pro377=)
Allele change: Synonymous_P377P

Associated conditions / phenotypes

Primary ciliary dyskinesia 9|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.