Variant (rsID / SNP)

rs9959080

rs9959080 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCBE1. Location: chromosome 18, position 57,100,768. Clinical significance in the table: Benign.

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Reference-table entries

CCBE1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:57100768
Cytoband: 18q21.32
HGVS: NM_133459.4(CCBE1):c.*2372C>T
Allele change: Silent

Associated conditions / phenotypes

Hennekam lymphangiectasia-lymphedema syndrome 1

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.