ClinVar Miner

Variants studied for Rhabdoid tumor predisposition syndrome 1

Coded as:
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 total
10 1 32 8 16 66

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
SMARCB1 10 1 32 5 15 62
SMARCE1 0 0 0 3 1 4

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 15 3 14 32
Baylor Genetics 1 0 15 0 0 16
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 5 4 9
Invitae 3 1 2 0 0 6
OMIM 3 0 0 0 0 3
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 0 0 0 1
Genetics and Molecular Pathology, SA Pathology 1 0 0 0 0 1
Department of Pediatrics, Memorial Sloan Kettering Cancer Center 1 0 0 0 0 1
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 1 0 0 1

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