ClinVar Miner

Variants studied for Lissencephaly, X-linked

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
12 5 1 0 0 18

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
DCX 12 5 1 18

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 8 0 0 8
Genetic Services Laboratory, University of Chicago 2 0 0 2
Baylor Genetics 0 0 1 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 1 0 1
Blueprint Genetics 0 1 0 1
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 1 0 1
NeuroMeGen,Hospital Clinico Santiago de Compostela 0 1 0 1
Génétique des Maladies du Développement, Hospices Civils de Lyon 1 0 0 1
Broad Institute Rare Disease Group,Broad Institute 0 1 0 1
Cavalleri Lab, Royal College of Surgeons in Ireland 1 0 0 1

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