Variant (rsID / SNP)

rs199768005

rs199768005 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,412,314. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

APOEBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:45412314
Cytoband: 19q13.32
HGVS: NM_000041.4(APOE):c.761T>A (p.Val254Glu)
Allele change: Missense_V254E

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.