Variant (rsID / SNP)

rs150655393

rs150655393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ODAD2. Location: chromosome 10, position 28,149,640. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ODAD2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:28149640
Cytoband: 10p12.1
HGVS: NM_018076.5(ODAD2):c.2935G>A (p.Val979Met)
Allele change: Missense_V504M

Associated conditions / phenotypes

Primary ciliary dyskinesia 23

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.