Variant (rsID / SNP)
rs6590358
rs6590358 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ5. Location: chromosome 11, position 128,787,964. Clinical significance in the table: Benign.
Reference-table entries
KCNJ5Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:128787964
- Cytoband
- 11q24.3
- HGVS
- NM_000890.5(KCNJ5):c.*1338C>A
- Allele change
- Silent
Associated conditions / phenotypes
Familial hyperaldosteronism|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.