ClinVar Miner

Variants studied for Methylcobalamin deficiency type cblE

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 not provided total
76 30 159 481 51 1 780

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 not provided total
MTRR 76 30 159 481 50 1 779
LOC129993631, MTRR 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 14
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 70 23 140 479 42 0 754
Natera, Inc. 4 4 29 18 25 0 80
Pars Genome Lab 0 0 0 0 11 0 11
Revvity Omics, Revvity 0 3 6 0 0 0 9
Genome-Nilou Lab 0 0 0 0 8 0 8
OMIM 6 0 0 0 0 0 6
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 3 1 0 0 0 0 4
Baylor Genetics 0 0 3 0 0 0 3
Mendelics 3 0 0 0 0 0 3
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 1 0 0 0 2
3billion 1 0 1 0 0 0 2
GenomeConnect, ClinGen 0 0 0 0 0 1 1
New York Genome Center 0 0 1 0 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 0 0 0 0 1

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