Variant (rsID / SNP)

rs61752469

rs61752469 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDC14A. Location: chromosome 1, position 100,964,774. Clinical significance in the table: Benign.

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Reference-table entries

CDC14ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:100964774
Cytoband: 1p21.2
HGVS: NM_003672.4(CDC14A):c.1711G>A (p.Gly571Arg)
Allele change: Missense_G513R

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.