Variant (rsID / SNP)

rs142289528

rs142289528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDC6. Location: chromosome 17, position 38,445,837. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDC6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:38445837
Cytoband: 17q21.2
HGVS: NM_001254.4(CDC6):c.165C>T (p.Pro55=)
Allele change: Synonymous_P55P

Associated conditions / phenotypes

Meier-Gorlin syndrome 5

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.