Variants studied for arterial calcification, generalized, of infancy, 2

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
30	17	102	60	59	261

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	total
ABCC6	30	17	99	60	59	258
ABCC6, LOC125146421	0	0	3	0	0	3

Submitter and significance breakdown #

Total submitters: 7

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	25	14	99	60	7	205
Genome-Nilou Lab	0	0	0	0	57	57
OMIM	8	0	0	0	0	8
Centre for Mendelian Genomics, University Medical Centre Ljubljana	2	3	1	0	0	6
Baylor Genetics	2	0	3	0	0	5
MGZ Medical Genetics Center	0	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1

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