Variant (rsID / SNP)

rs5065

rs5065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPPA. Location: chromosome 1, position 11,906,068. Clinical significance in the table: Benign.

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Reference-table entries

NPPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:11906068
Cytoband: 1p36.22
HGVS: NM_006172.4(NPPA):c.454T>C (p.Ter152Arg)
Allele change: Silent

Associated conditions / phenotypes

Atrial fibrillation, familial, 6

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.