ClinVar Miner

Variants studied for Primary dilated cardiomyopathy; Hypertrophic cardiomyopathy

Coded as:
Minimum submission review status: Collection method:
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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 not provided total
3 0 201 83 22 1 310

Gene and significance breakdown #

Total genes and gene combinations: 9
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Gene or gene combination pathogenic uncertain significance likely benign benign not provided total
PDLIM3 0 183 76 18 0 277
LOC126807246, PDLIM3 0 14 7 4 0 25
ACTN2 1 0 0 0 1 2
ANKRD37, CCDC110, CFAP96, CFAP97, LOC105377590, LOC121056754, LOC123493248, LOC123493249, LOC123493250, LOC126807246, LOC129993502, LOC129993503, LOC129993504, LOC129993505, LOC129993506, LOC129993507, LOC129993508, LOC129993509, LOC129993510, LOC129993511, LOC129993512, LOC129993513, LOC129993514, LOC129993515, LOC129993516, LOC129993517, LOC129993518, LOC129993519, LOC129993520, LOC129993521, LOC129993522, LOC129993523, LRP2BP, PDLIM3, SLC25A4, SNX25, UFSP2 0 1 0 0 0 1
ANKRD37, CCDC110, CFAP96, CFAP97, LRP2BP, PDLIM3, SLC25A4, SNX25, UFSP2 0 1 0 0 0 1
CCDC110, PDLIM3 0 1 0 0 0 1
MYBPC3 1 0 0 0 0 1
MYH7 0 1 0 0 0 1
TNNT2 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic uncertain significance likely benign benign not provided total
Invitae 0 200 83 22 0 305
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 2 0 0 0 0 2
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 1 1 0 0 0 2
GenomeConnect, ClinGen 0 0 0 0 1 1

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