Variant (rsID / SNP)
rs61757663
rs61757663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,726,527. Clinical significance in the table: Likely benign.
Reference-table entries
AKAP9Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:91726527
- Cytoband
- 7q21.2
- HGVS
- NM_005751.5(AKAP9):c.10254G>C (p.Gln3418His)
- Allele change
- Missense_Q3410H
Associated conditions / phenotypes
Long QT syndrome 11|Long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.