Variant (rsID / SNP)

rs4373934

rs4373934 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNJ5. Location: chromosome 11, position 128,787,405. 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: 11:128787405
Cytoband: 11q24.3
HGVS: NM_000890.5(KCNJ5):c.*779G>T
Allele change: Silent

Associated conditions / phenotypes

Congenital long QT syndrome|Familial hyperaldosteronism type III

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.