Variant (rsID / SNP)

rs28936379

rs28936379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSEN2. Location: chromosome 1, position 227,076,678. Clinical significance in the table: Pathogenic.

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Reference-table entries

PSEN2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:227076678
Cytoband: 1q42.13
HGVS: NM_000447.3(PSEN2):c.715A>G (p.Met239Val)
Allele change: Missense_M239V

Associated conditions / phenotypes

Alzheimer disease 4

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.