Annotation Detail
Information
- Associated Genes
- KCNQ1
- Associated Variants
-
KCNQ1 p.Arg452Gln (p.R452Q)
(
ENST00000496887.7,
ENST00000155840.12,
ENST00000646564.2,
ENST00000335475.6,
ENST00000713725.1 )
KCNQ1 p.Arg452Gln (p.R452Q) ( ENST00000155840.12, ENST00000335475.6, ENST00000496887.7, ENST00000646564.2, ENST00000713725.1 ) - Associated Disease
- Short QT syndrome type 2 Atrial fibrillation, familial, 3 long QT syndrome 1
- Source Database
- ClinVar
- Description
- NM_000218.3(KCNQ1):c.1355G>A (p.Arg452Gln) AND multiple conditions
- ClinVar Allele ID
- 77926
- ClinVar RefSeq Alternation Syntax
- NM_000218.3:c.1355G>A
- ClinVar RefSeq Alternation Syntax
- NM_001406836.1:c.1259G>A
- ClinVar RefSeq Alternation Syntax
- NM_001406837.1:c.1085G>A
- ClinVar RefSeq Alternation Syntax
- NM_181798.2:c.974G>A
- ClinVar RefSeq Alternation Syntax
- NM_001406838.1:c.815G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-05-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003448257
- ClinVar Disease
- Long QT syndrome 1
- ClinVar Disease
- Atrial fibrillation, familial, 3
- ClinVar Disease
- Short QT syndrome type 2
- Observed Origin Sample
- germline
Drugs