Variants studied for Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type

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	1	301	83	4	389

Gene and significance breakdown #

Total genes and gene combinations: 8

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
FN1	1	1	240	60	3	304
ATIC, FN1	0	0	23	4	0	27
FN1, LOC126806498	0	0	7	7	0	14
FN1, LOC126806497	0	0	9	3	1	13
FN1, LOC126806496	0	0	6	5	0	11
FN1, LOC122861289	0	0	6	3	0	9
FN1, FN1-DT	0	0	6	0	0	6
FN1, LOC126806499	0	0	4	1	0	5

Submitter and significance breakdown #

Total submitters: 3

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	1	1	299	79	4	384
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	2	4	0	6
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	0	0	1

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