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Variant (rsID / SNP)

rs972201049

KCNH2

rs972201049 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,652,569. 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
7:150652569
Cytoband
7q36.1
HGVS
NM_000238.4(KCNH2):c.1128+1810C>T
Allele change
Missense_A8V

Associated conditions / phenotypes

Short QT syndrome type 1|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.