Variant (rsID / SNP)

rs794728476

rs794728476 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,671,853. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KCNH2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Duplication
Chromosome / position: 7:150671853
Cytoband: 7q36.1
HGVS: NM_000238.4(KCNH2):c.244_252dup (p.Gln84_Ala85insIleAlaGln)

Associated conditions / phenotypes

Cardiac arrhythmia

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.