Variants studied for Ventricular fibrillation, paroxysmal familial, type 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	total
1	3	146	32	15	197

Gene and significance breakdown #

Total genes and gene combinations: 14

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
SCN5A	1	0	123	28	13	165
LOC110121269, SCN5A	0	0	12	3	2	17
JUP	0	0	2	0	0	2
RBM20	0	0	2	0	0	2
RYR2	0	2	0	0	0	2
CACNA1C	0	1	0	0	0	1
DPP6	0	0	1	0	0	1
DSP	0	0	1	0	0	1
KCNH2	0	0	1	0	0	1
MYH7	0	0	0	1	0	1
PKP2	0	0	1	0	0	1
SNTA1	0	0	1	0	0	1
TTN	0	0	1	0	0	1
VCL	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 4

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	135	31	15	181
Blueprint Genetics	0	3	10	2	0	15
OMIM	1	0	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	0	1

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