Variants in gene LRRC56 - ClinVar Miner

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
12	5	123	149	55	323

Condition and significance breakdown #

Total conditions: 4

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
not provided	9	3	97	131	55	291
LRRC56-related condition	0	0	1	28	18	47
Inborn genetic diseases	0	0	37	3	0	40
Ciliary dyskinesia, primary, 39	4	2	3	3	10	22

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Invitae	9	3	97	127	36	272
PreventionGenetics, part of Exact Sciences	0	0	1	28	18	47
Ambry Genetics	0	0	37	3	0	40
GeneDx	0	0	0	0	28	28
CeGaT Center for Human Genetics Tuebingen	0	0	0	6	6	12
Genome-Nilou Lab	0	0	0	0	9	9
OMIM	4	0	0	0	0	4
Fulgent Genetics, Fulgent Genetics	0	0	0	3	1	4
Revvity Omics, Revvity	0	0	2	0	0	2
Baylor Genetics	0	1	0	0	0	1
Genetics and Molecular Pathology, SA Pathology	0	0	1	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	0	0	0	1

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