ClinVar Miner

Variants studied for Fanconi renotubular syndrome 2

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
9 24 117 16 4 164

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 total
SLC34A1 9 24 117 16 4 164

Submitter and significance breakdown #

Total submitters: 11
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 3 14 105 16 2 140
Rare Kidney Stone Consortium and the Mayo Clinic Hyperoxaluria Center, Mayo Clinic 4 7 8 0 0 19
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 2 1 0 3
First Genomix Gene Laboratory, Genetic Diagnostics Department 1 2 0 0 0 3
3billion 0 0 2 0 0 2
Genome-Nilou Lab 0 0 0 0 2 2
Arcensus 0 1 0 0 0 1
Dubai Health Genomic Medicine Center, Dubai Health 0 1 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
Laboratory of Cyto-molecular Genetics, Department of Anatomy, All India Institute of Medical Sciences (AIIMS), New Delhi 0 1 0 0 0 1
OMIM 1 0 0 0 0 1

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