ClinVar Miner

Variants studied for Myofibrillar myopathy, ZASP-related

Coded as:
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 0 282 148 46 468

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
LDB3 1 247 135 39 414
LDB3, LOC110121486 3 35 13 7 54

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Invitae 2 250 141 45 438
Illumina Clinical Services Laboratory,Illumina 0 31 7 0 38
OMIM 3 0 0 0 3
Mendelics 0 2 0 1 3
GeneReviews 1 0 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 1 0 0 1

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