Variant (rsID / SNP)
rs61757261
rs61757261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPPA, NPPA-AS1. Location: chromosome 1, position 11,907,430. Clinical significance in the table: Benign.
Reference-table entries
NPPABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:11907430
- Cytoband
- 1p36.22
- HGVS
- NM_006172.4(NPPA):c.190A>C (p.Ser64Arg)
- Allele change
- Silent
Associated conditions / phenotypes
Atrial fibrillation, familial, 6
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.