ClinVar Miner

Variants in gene ARVCF

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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
0 0 134 17 59 207

Condition and significance breakdown #

Total conditions: 5
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Condition uncertain significance likely benign benign total
not specified 126 1 0 127
not provided 7 15 59 79
Long QT syndrome 0 1 0 1
Microcephaly 1 0 0 1
See cases 1 0 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter uncertain significance likely benign benign total
Ambry Genetics 126 1 0 127
Breakthrough Genomics, Breakthrough Genomics 0 4 46 50
GeneDx 0 0 48 48
Labcorp Genetics (formerly Invitae), Labcorp 0 7 13 20
CeGaT Center for Human Genetics Tuebingen 6 10 1 17
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 0 1 0 1
Medical Research Institute, Tokyo Medical and Dental University 0 1 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 0 1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System 1 0 0 1
Department of Pediatrics, Samsung Medical Center, Samsung Medical Center 1 0 0 1

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