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Variant (rsID / SNP)

rs8076604

MYO18A

rs8076604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO18A. Location: chromosome 17, position 27,438,469. The table records no clinical significance for this variant.

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Reference-table entries

MYO18ANot classified
Variant type
missense_variant
Chromosome / position
17:27438469
HGVS
NM_001346765.2,c.2930C>T,p.Ala977Val
Allele change
Missense_A958V

Associated conditions / phenotypes

Alzheimer Disease

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.