Variant (rsID / SNP)
rs755408339
rs755408339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,603,095. 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
- 7:91603095
- Cytoband
- 7q21.2
- HGVS
- NM_005751.5(AKAP9):c.119G>A (p.Arg40Lys)
- Allele change
- Missense_R40K
Associated conditions / phenotypes
Congenital long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.