ClinVar Miner

Variants studied for Nephrotic syndrome, idiopathic, steroid-resistant

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
24 37 23 2 8 87

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
NPHS2 18 23 13 2 2 54
AXDND1, NPHS2 6 14 10 0 6 33

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Counsyl 8 33 20 2 0 63
OMIM 10 0 0 0 0 10
Human Genetics Disease in Children – Taif University,Taif University 3 1 0 0 4 8
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 6 2 0 0 0 8
Fulgent Genetics,Fulgent Genetics 2 1 0 0 0 3
Athena Diagnostics Inc 0 0 0 0 2 2
Illumina Clinical Services Laboratory,Illumina 2 0 0 0 0 2
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 0 0 0 2 2
Department of Genetics,Sultan Qaboos University Hospital, Oman 1 0 1 0 0 2
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 0 1 0 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 0 1 0 0 1
Tehran Medical Genetics Laboratory 0 1 0 0 0 1

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