ClinVar Miner

Variants studied for arthrogryposis, distal, type 1B

Included ClinVar conditions (2):
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 1 24 6 47 77

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
MYBPC1 2 1 22 6 45 73
LOC105369937, MYBPC1 0 0 2 0 2 4

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 21 4 43 68
Genome-Nilou Lab 0 0 0 0 9 9
Fulgent Genetics, Fulgent Genetics 0 0 1 2 0 3
OMIM 2 0 0 0 0 2
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 0 1 0 0 1
Institute of Human Genetics, Heidelberg University 0 1 0 0 0 1
Suma Genomics 0 0 1 0 0 1

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