Variants studied for renal dysplasia, cystic, susceptibility to

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	risk factor	total
2	4	15	2	2	2	27

Gene and significance breakdown #

Total genes and gene combinations: 4

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
BICC1	2	3	13	2	2	2	24
ACE	0	0	1	0	0	0	1
AGTR1	0	0	1	0	0	0	1
BICC1, LOC126860938	0	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
Fulgent Genetics, Fulgent Genetics	0	0	6	2	2	0	10
MVZ Medizinische Genetik Mainz	0	4	1	0	0	0	5
Johns Hopkins Genomics, Johns Hopkins University	0	0	3	0	0	0	3
OMIM	0	0	0	0	0	2	2
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	0	2	0	0	0	2
Molecular Genetics laboratory, Necker Hospital	0	0	2	0	0	0	2
MGZ Medical Genetics Center	0	0	1	0	0	0	1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	1	0	0	0	0	0	1
Prenatal Diagnosis Center, Inner Mongolia Medical University	1	0	0	0	0	0	1
Regional Center For Medical Genetics Timis, Louis Turcanu Emergency Hospital for Children Timisoara	0	0	1	0	0	0	1

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