ClinVar Miner

Variants in gene combination AP3M1, VCL

See also:
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 6 1 1 8

Condition and significance breakdown #

Total conditions: 4
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Condition uncertain significance likely benign benign total
Dilated Cardiomyopathy, Dominant 3 0 0 3
Dilated cardiomyopathy 1W 1 1 1 3
Dilated cardiomyopathy 1W; Familial hypertrophic cardiomyopathy 15 1 0 0 1
not provided 1 0 0 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 4 1 1 6
Lineagen, Inc 1 0 0 1
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 1 0 0 1

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