ClinVar Miner

Variants studied for autoimmune lymphoproliferative syndrome type 2A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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