Variant (rsID / SNP)

rs748706373

rs748706373 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,644,699. Clinical significance in the table: Pathogenic.

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Reference-table entries

KCNH2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 7:150644699
Cytoband: 7q36.1
HGVS: NM_000238.4(KCNH2):c.2959_2960del (p.Leu987fs)

Associated conditions / phenotypes

Cardiovascular phenotype|Long QT syndrome|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.