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 0 286 124 56 4 452

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 2 285 124 56 4 451
CASP10, LOC129935405 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic uncertain significance likely benign benign not provided total
Invitae 0 229 118 19 0 366
Illumina Laboratory Services, Illumina 0 59 8 46 0 113
Revvity Omics, Revvity 0 7 0 0 0 7
Baylor Genetics 0 4 0 0 0 4
GeneReviews 0 0 0 0 4 4
OMIM 1 1 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
Mendelics 1 0 0 0 0 1
Fulgent Genetics, Fulgent Genetics 0 1 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 1 0 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 0 0 0 1

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