ClinVar Miner

Variants studied for Intellectual developmental disorder with severe speech and ambulation defects

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
3 4 4 0 1 8

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
ACTL6B 3 4 4 1 8

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 2 0 0 0 2
SIB Swiss Institute of Bioinformatics 0 1 1 0 2
MGZ Medical Genetics Center 0 1 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 1
Institute of Human Genetics, University of Leipzig Medical Center 1 0 0 0 1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 1 0 0 0 1
Genome-Nilou Lab 0 0 0 1 1
3billion 0 1 0 0 1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 0 1 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 0 1 0 1
Houlden Lab, UCL Institute of Neurology 1 0 0 0 1
Laboratory of genome editing, Research Centre for Medical Genetics 0 1 0 0 1

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