Variant (rsID / SNP)

rs114128928

rs114128928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDK5RAP2. Location: chromosome 9, position 123,156,914. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CDK5RAP2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 9:123156914
Cytoband: 9q33.2
HGVS: NM_018249.6(CDK5RAP2):c.5454T>G (p.Ile1818Met)
Allele change: Silent

Associated conditions / phenotypes

Primary Microcephaly, Recessive

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.