Variant (rsID / SNP)
rs766379103
rs766379103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,671,918. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
KCNH2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:150671918
- Cytoband
- 7q36.1
- HGVS
- NM_000238.4(KCNH2):c.188C>A (p.Pro63His)
- Allele change
- Missense_P63H
Associated conditions / phenotypes
Long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.