Variants studied for Polycystic kidney disease 6 with or without polycystic liver disease

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
6	2	5	0	1	12

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
DNAJB11	6	2	5	1	12

Submitter and significance breakdown #

Total submitters: 7

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
OMIM	5	0	0	0	5
SIB Swiss Institute of Bioinformatics	1	2	0	0	3
Revvity Omics, Revvity	0	0	2	0	2
Institute of Human Genetics, Cologne University	0	0	2	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	0	1	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	0	1	1

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