Variant (rsID / SNP)

rs199473522

rs199473522 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,648,671. Clinical significance in the table: Pathogenic.

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Reference-table entries

KCNH2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:150648671
Cytoband: 7q36.1
HGVS: NM_000238.4(KCNH2):c.1810G>A (p.Gly604Ser)
Allele change: Missense_G264S

Associated conditions / phenotypes

Congenital long QT syndrome|Long QT syndrome|Inborn genetic diseases

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.