Variant (rsID / SNP)

rs45516097

rs45516097 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ5. Location: chromosome 11, position 128,782,112. Clinical significance in the table: Benign.

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Reference-table entries

KCNJ5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:128782112
Cytoband: 11q24.3
HGVS: NM_000890.5(KCNJ5):c.937+7C>T
Allele change: Silent

Associated conditions / phenotypes

Familial hyperaldosteronism type III|Congenital long QT syndrome|Long QT syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.