SNP rs534584472


Genomic Context

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Variant Effect Impact (snpEff)

  • High
  • Moderate
  • Low
  • Modifier
  • Not Reported
  • Reference Allele: C
  • Minor Allele/Frequency: T/0.001797
  • Variant Class: single nucleotide variant
  • Closest Gene: APOE

Genome-wide significance

NIAGADS: Alzheimer's Disease

NIAGADS: Related Neuropathologies

NHGRI: Alzheimer's Disease

NHGRI: Other Traits

Predicted Effects