Variant (rsID / SNP)
rs185898118
rs185898118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP9. Location: chromosome 7, position 91,622,234. 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
- 7:91622234
- Cytoband
- 7q21.2
- HGVS
- NM_005751.5(AKAP9):c.441A>T (p.Glu147Asp)
- Allele change
- Missense_E147D
Associated conditions / phenotypes
Long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.