ClinVar Miner

Variants studied for Osteoporosis with pseudoglioma

Coded as:
Minimum submission review status: Collection method:
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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
21 11 6 1 1 1 38

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
LRP5 21 11 6 1 1 1 38

Submitter and significance breakdown #

Total submitters: 11
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
OMIM 19 0 0 0 0 0 19
Baylor Genetics 0 0 3 0 0 0 3
Mendelics 0 1 0 1 1 0 3
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 3 0 0 0 0 3
3billion 2 1 0 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 1 0 0 0 1 2
Genetics Department, Polish Mother's Memorial Hospital Research Institute 0 2 0 0 0 0 2
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 1 1 0 0 0 2
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 2 0 0 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 1 0 0 0 0 1
Breda Genetics srl 0 1 0 0 0 0 1

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