ClinVar Miner

Variants studied for Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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Minimum submission review status: Collection method:
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Gene type:
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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
20 1 34 46 24 121

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
NOTCH3 20 1 34 45 24 120
MIR6795, NOTCH3 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 2 0 32 46 21 101
OMIM 12 0 0 0 0 12
Athena Diagnostics Inc 0 0 0 0 5 5
GeneReviews 3 0 0 0 0 3
Mendelics 2 0 0 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 0 2 0 0 2
Molecular Diagnostics Laboratory,M Health: University of Minnesota 1 1 0 0 0 2
ClinVar Staff, National Center for Biotechnology Information (NCBI) 1 0 0 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 1 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 1 0 0 0 0 1

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