ClinVar Miner

Variants studied for cardiac valvular defect, developmental

Included ClinVar conditions (1):
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
4 9 12 0 2 27

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
PLD1 4 9 12 2 27

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance benign total
Baylor Genetics 0 4 5 0 9
Revvity Omics, Revvity 0 0 4 0 4
OMIM 3 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 1 0 0 2
Fulgent Genetics, Fulgent Genetics 0 1 1 0 2
Genome-Nilou Lab 0 0 0 2 2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 0 1 0 1
Diagnostics Division, CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS 0 1 0 0 1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 1 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 1
Lifecell International Pvt. Ltd 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 1

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