Variant (rsID / SNP)

rs9827878

rs9827878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP63. Location: chromosome 3, position 134,225,969. Clinical significance in the table: Benign.

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Reference-table entries

CEP63Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:134225969
Cytoband: 3q22.2
HGVS: NM_001353108.3(CEP63):c.63T>C (p.Cys21=)
Allele change: Synonymous_C21C

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.