Variants in gene LIMS2 - 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
2	2	183	120	47	350

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Autosomal recessive limb-girdle muscular dystrophy type 2W	2	2	165	109	17	294
not specified	0	0	48	4	3	55
not provided	0	0	3	8	36	46
LIMS2-related disorder	0	0	1	5	1	7
Decreased total neutrophil count; Decreased total lymphocyte count	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	0	0	150	111	17	278
Revvity Omics, Revvity	0	0	56	1	0	57
Ambry Genetics	0	0	48	1	0	49
GeneDx	0	0	0	0	31	31
Breakthrough Genomics, Breakthrough Genomics	0	0	1	2	26	29
PreventionGenetics, part of Exact Sciences	0	0	1	8	4	13
CeGaT Center for Human Genetics Tuebingen	0	0	2	4	1	7
OMIM	2	0	0	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	1	0	0	2
Kariminejad - Najmabadi Pathology & Genetics Center	0	0	2	0	0	2
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	1	0	0	1
Johns Hopkins Genomics, Johns Hopkins University	0	0	1	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1
Department of Biosciences, University of Milan	0	0	1	0	0	1

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