Variant (rsID / SNP)

rs869312849

rs869312849 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSNK2A1. Location: chromosome 20, position 485,826. Clinical significance in the table: Pathogenic.

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Reference-table entries

CSNK2A1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 20:485826
Cytoband: 20p13
HGVS: NM_177559.3(CSNK2A1):c.149A>C (p.Tyr50Ser)
Allele change: Missense_Y50S

Associated conditions / phenotypes

Okur-Chung neurodevelopmental syndrome

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.