ClinVar Miner

Variants studied for Diaphyseal medullary stenosis-bone malignancy syndrome

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
2 0 65 3 56 126

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
MTAP 0 65 3 56 124
ERVFRD-3, MTAP 2 0 0 0 2

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services,Illumina 0 63 3 56 122
OMIM 2 0 0 0 2
Mendelics 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 0 0 1
Clinical Genetics Laboratory,University Hospital Schleswig-Holstein 0 1 0 0 1

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