Variants in gene ANKS3 - ClinVar Miner

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
1	0	93	12	5	110

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	uncertain significance	likely benign	benign	total
not specified	0	91	6	0	97
not provided	0	2	5	5	11
ANKS3-related disorder	0	0	2	0	2
Non-immune hydrops fetalis	0	1	0	0	1
Short stature	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	91	6	0	97
Breakthrough Genomics, Breakthrough Genomics	0	2	1	5	8
Labcorp Genetics (formerly Invitae), Labcorp	0	0	1	5	6
CeGaT Center for Human Genetics Tuebingen	0	0	4	0	4
PreventionGenetics, part of Exact Sciences	0	0	2	0	2
OMIM	0	1	0	0	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	0	0	1
Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg	1	0	0	0	1

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