Variants in gene KIAA0825

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
5	2	32	7	16	58

Condition and significance breakdown #

Total conditions: 7

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
KIAA0825-related disorder	0	0	4	5	16	25
not specified	0	0	23	2	0	25
Polydactyly, postaxial, type a10	5	0	4	0	2	11
not provided	0	0	3	0	1	4
Autosomal recessive nonsyndromic postaxial polydactyly	0	2	0	0	0	2
Polydactyly, postaxial, type A1	2	0	0	0	0	2
See cases	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	0	23	2	0	25
PreventionGenetics, part of Exact Sciences	0	0	4	5	16	25
OMIM	3	0	0	0	0	3
GeneDx	0	0	3	0	0	3
University of Washington Center for Mendelian Genomics, University of Washington	0	2	0	0	0	2
Center for Statistical Genetics, Columbia University	2	0	0	0	0	2
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	2	0	0	2
Genome-Nilou Lab	0	0	0	0	2	2
Intergen, Intergen Genetics and Rare Diseases Diagnosis Center	0	0	1	0	0	1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	0	0	0	0	1
ISCA site 1	0	0	1	0	0	1
CeGaT Center for Human Genetics Tuebingen	0	0	0	0	1	1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	1	0	0	0	0	1
3billion	0	0	1	0	0	1

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