Variant (rsID / SNP)

rs118010078

rs118010078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASPM. Location: chromosome 1, position 197,070,906. 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: 1:197070906
Cytoband: 1q31.3
HGVS: NM_018136.5(ASPM):c.7475G>A (p.Arg2492Lys)
Allele change: Silent

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.