Variant (rsID / SNP)

rs145999145

rs145999145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLD3. Location: chromosome 19, position 40,877,595. Clinical significance in the table: Likely benign.

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Reference-table entries

PLD3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:40877595
Cytoband: 19q13.2
HGVS: NM_012268.4(PLD3):c.694G>A (p.Val232Met)
Allele change: Missense_V232M

Associated conditions / phenotypes

Alzheimer disease 19

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.