ClinVar Miner

Variants studied for Dilated cardiomyopathy 1O

Coded as:
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
9 2 683 550 59 1265

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
ABCC9 9 2 680 550 59 1262
ABCC9, GOLT1B, GYS2, KCNJ8, LDHB, PYROXD1, RECQL, SPX 0 0 2 0 0 2
ABCC9, KCNJ8 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 7 1 639 542 59 1248
Illumina Laboratory Services, Illumina 0 0 46 8 5 59
Mendelics 0 0 1 0 2 3
OMIM 2 0 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 2 0 0 2
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 2 0 0 2
Baylor Genetics 0 1 0 0 0 1
MGZ Medical Genetics Center 0 0 1 0 0 1
Mayo Clinic Laboratories, Mayo Clinic 0 0 1 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 0 1
Servicio Canario de Salud, Hospital Universitario Nuestra Sra. de Candelaria 0 0 1 0 0 1

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