Variants studied for neurohypophyseal diabetes insipidus

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	uncertain risk allele	total
19	4	2	4	0	2	28

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	uncertain risk allele	total
AVP	19	4	2	4	2	28

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	uncertain risk allele	total
OMIM	18	0	0	0	0	18
Fulgent Genetics, Fulgent Genetics	2	0	0	4	0	6
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic	0	0	1	0	2	3
Institute of Human Genetics, University of Leipzig Medical Center	1	1	0	0	0	2
Revvity Omics, Revvity	0	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	0	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	1	0	0	0	1
MVZ Medizinische Genetik Mainz	0	1	0	0	0	1

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