Variant (rsID / SNP)

rs150949692

rs150949692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC65. Location: chromosome 12, position 49,312,251. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC65Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 12:49312251
Cytoband: 12q13.12
HGVS: NM_033124.5(CCDC65):c.803T>C (p.Leu268Pro)
Allele change: Missense_L125P

Associated conditions / phenotypes

Primary ciliary dyskinesia 27

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.