Gene: KCNQ1-AS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR Large deletion in KCNQ1 identified in a family with Jervell and Lange-Nielsen syndrome. 25187895 2014
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. 23631430 2013
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. 23098067 2012
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome. 19825999 2009
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome. 16981927 2006
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 CausalMutation disease CLINVAR Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. 10024302 1999
Entrez Id: 338653
Gene Symbol: KCNQ1-AS1
KCNQ1-AS1 		0.100 GeneticVariation disease CLINVAR