Variants studied for blastoma

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
10	7	26	22	20	1	85

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
DICER1	10	7	26	22	20	1	85

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
KCCC/NGS Laboratory, Kuwait Cancer Control Center	0	0	0	8	16	0	24
Illumina Laboratory Services, Illumina	0	0	7	6	4	0	17
St. Jude Molecular Pathology, St. Jude Children's Research Hospital	3	0	13	0	0	0	16
Fulgent Genetics, Fulgent Genetics	1	0	4	9	1	0	15
OMIM	6	0	0	0	0	0	6
MGZ Medical Genetics Center	0	1	2	0	0	0	3
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	2	0	0	0	0	3
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research	0	2	0	0	0	0	2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	1	0	0	0	0	1
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	1	1
MVZ Medizinische Genetik Mainz	0	1	0	0	0	0	1

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