Variants studied for Migraine, familial hemiplegic, 3

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
25	11	62	20	22	4	138

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
LOC102724058, SCN1A	13	4	42	11	16	4	85
SCN1A	12	7	20	9	6	0	53

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Illumina Laboratory Services, Illumina	0	0	58	19	22	0	99
Centre for Mendelian Genomics, University Medical Centre Ljubljana	8	8	2	1	0	0	19
Center of Excellence for Medical Genomics, Chulalongkorn University	11	2	0	0	0	0	13
UniProtKB/Swiss-Prot	0	0	0	0	0	4	4
OMIM	3	0	0	0	0	0	3
DASA	3	0	0	0	0	0	3
Baylor Genetics	0	0	2	0	0	0	2
Clinical Genetics and Genomics, Karolinska University Hospital	0	1	0	0	0	0	1

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