Variants studied for sick sinus syndrome 1

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	not provided	total
20	15	287	26	50	1	389

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
SCN5A	19	14	254	23	43	1	346
LOC110121269, SCN5A	1	1	33	3	7	0	43

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	12	6	162	10	5	0	195
Illumina Laboratory Services, Illumina	0	0	119	16	47	0	182
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	15	0	0	0	15
Juno Genomics, Hangzhou Juno Genomics, Inc	1	6	3	0	0	0	10
Centre for Mendelian Genomics, University Medical Centre Ljubljana	2	1	5	0	0	0	8
OMIM	4	0	0	0	0	0	4
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	2	0	0	0	0	0	2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	1	0	0	0	0	0	1
New York Genome Center	0	0	1	0	0	0	1
Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital	0	1	0	0	0	0	1
DASA	1	0	0	0	0	0	1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center	0	1	0	0	0	0	1
GenomeConnect - Brain Gene Registry	0	0	0	0	0	1	1

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