Variants studied for thyrotoxic periodic paralysis, susceptibility to, 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	risk factor	total
1	8	186	167	72	3	425

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
CACNA1S	1	8	186	167	72	3	425

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
Genome-Nilou Lab	0	1	115	150	72	0	338
Fulgent Genetics, Fulgent Genetics	1	8	140	81	3	0	233
OMIM	0	0	0	0	0	3	3
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	0	1

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