Variant (rsID / SNP)

rs1805123

rs1805123 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,645,534. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KCNH2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:150645534
Cytoband: 7q36.1
HGVS: NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr)
Allele change: Missense_K557T

Associated conditions / phenotypes

Atrial fibrillation|Cardiovascular phenotype|Long QT syndrome|Long QT syndrome 2|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.