Variants studied for autoimmune lymphoproliferative syndrome type 2A

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
2	0	329	140	56	4	511

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	uncertain significance	likely benign	benign	not provided	total
CASP10	2	328	140	56	4	510
CASP10, LOC129935405	0	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	0	269	134	19	0	422
Illumina Laboratory Services, Illumina	0	59	8	46	0	113
Revvity Omics, Revvity	0	7	0	0	0	7
Department of Pathology and Laboratory Medicine, Sinai Health System	0	6	0	0	0	6
Baylor Genetics	0	4	0	0	0	4
GeneReviews	0	0	0	0	4	4
OMIM	1	1	0	0	0	2
Fulgent Genetics, Fulgent Genetics	0	2	0	0	0	2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	2	0	0	0	2
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	0	2	0	0	0	2
Genome-Nilou Lab	0	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	2	0	0	0	2
Mendelics	1	0	0	0	0	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	1	0	0	0	1

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