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Variant (rsID / SNP)

rs201627778

KCNH2

rs201627778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,645,550. 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
single nucleotide variant
Chromosome / position
7:150645550
Cytoband
7q36.1
HGVS
NM_000238.4(KCNH2):c.2674C>T (p.Arg892Cys)
Allele change
Missense_R552C

Associated conditions / phenotypes

Cardiovascular phenotype|Long QT syndrome 2|Long QT syndrome|Cardiac arrhythmia

Public references

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