Variants studied for Long QT syndrome 12

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
2	0	82	13	14	108

Gene and significance breakdown #

Total genes and gene combinations: 4

Download table as spreadsheet

Gene or gene combination	pathogenic	uncertain significance	likely benign	benign	total
SNTA1	2	66	12	12	89
LOC130065680, SNTA1	0	13	1	2	16
LOC130065679, SNTA1	0	2	0	0	2
LOC130065678, SNTA1	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 15

Download table as spreadsheet

Submitter	pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	39	8	12	59
Fulgent Genetics, Fulgent Genetics	0	42	2	1	45
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	5	3	5	13
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	4	0	0	4
OMIM	2	0	0	0	2
Revvity Omics, Revvity	0	2	0	0	2
Genome Diagnostics Laboratory, University Medical Center Utrecht	0	0	2	0	2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	2	0	0	2
Baylor Genetics	0	1	0	0	1
Institute of Human Genetics, University of Goettingen	0	1	0	0	1
Division of Human Genetics, Children's Hospital of Philadelphia	0	1	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	1	0	0	1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	0	0	1	0	1
Phosphorus, Inc.	0	1	0	0	1
Genome-Nilou Lab	0	0	0	1	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.