Variants studied for Steroid-resistant nephrotic syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
19	5	19	7	9	59

Gene and significance breakdown #

Total genes and gene combinations: 8

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
NPHS2	10	2	9	7	6	34
AXDND1, NPHS2	5	0	8	0	3	16
AVIL	3	0	0	0	0	3
CRB2	0	2	0	0	0	2
AVIL, TSFM	1	0	0	0	0	1
COL4A3, MFF-DT	0	0	1	0	0	1
COL4A4	0	0	1	0	0	1
COL4A5	0	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 6

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Natera, Inc.	14	2	15	7	9	47
Yale Center for Mendelian Genomics, Yale University	4	0	0	0	0	4
NIHR Bioresource Rare Diseases, University of Cambridge	0	3	0	0	0	3
Illumina Laboratory Services, Illumina	0	0	2	0	0	2
Diagnostics Division, CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS	0	0	2	0	0	2
Molecular Genetics, Royal Melbourne Hospital	1	0	1	0	0	2

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