Variant (rsID / SNP)

rs146561469

rs146561469 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASPM. Location: chromosome 1, position 197,111,915. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ASPMConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 1:197111915
Cytoband: 1q31.3
HGVS: NM_018136.5(ASPM):c.1467A>G (p.Arg489=)
Allele change: Synonymous_R489R

Associated conditions / phenotypes

Microcephaly 5, primary, autosomal 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.