ClinVar Miner

Variants studied for Deeah syndrome; Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia

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
0 3 7 1 1 12

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic uncertain significance likely benign benign total
MADD 3 7 1 1 12

Submitter and significance breakdown #

Total submitters: 8
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Submitter likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 0 1 0 1 2
Juno Genomics, Hangzhou Juno Genomics, Inc 1 1 0 0 2
New York Genome Center 0 2 0 0 2
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 2 0 0 2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 0 0 0 1
Department of Pathology and Laboratory Medicine, Sinai Health System 1 0 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 0 1
3billion 0 0 1 0 1

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