Variant (rsID / SNP)
rs61757557
rs61757557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,631,812. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
AKAP9Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:91631812
- Cytoband
- 7q21.2
- HGVS
- NM_005751.5(AKAP9):c.2581T>C (p.Tyr861His)
- Allele change
- Missense_Y861H
Associated conditions / phenotypes
Congenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.