ClinVar Miner

Variants studied for Neurofibromatosis, familial spinal

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
5 1 107 47 58 213

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
NF1 5 1 89 46 58 194
LOC111811965, MIR4733HG, NF1 0 0 18 1 0 19

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 107 24 29 160
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 23 39 62
OMIM 5 0 0 0 0 5
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 0 0 1

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