Variant (rsID / SNP)

rs377095107

rs377095107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNH2. Location: chromosome 7, position 150,644,429. Clinical significance in the table: Uncertain significance.

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Reference-table entries

KCNH2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:150644429
Cytoband: 7q36.1
HGVS: NM_000238.4(KCNH2):c.3139C>T (p.Arg1047Cys)
Allele change: Missense_R707C

Associated conditions / phenotypes

Long QT syndrome

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.