Variants in gene TNRC6A - 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	177	14	12	202

Condition and significance breakdown #

Total conditions: 3

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Condition	pathogenic	uncertain significance	likely benign	benign	total
not specified	0	172	3	0	175
not provided	0	4	11	12	27
Epilepsy, familial adult myoclonic, 6	1	3	0	6	10

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	172	3	0	175
Breakthrough Genomics, Breakthrough Genomics	0	0	1	10	11
Labcorp Genetics (formerly Invitae), Labcorp	0	0	3	6	9
CeGaT Center for Human Genetics Tuebingen	0	0	8	1	9
Genome-Nilou Lab	0	0	0	6	6
Department of Pathology and Laboratory Medicine, Sinai Health System	0	2	0	0	2
Clinical Genetics Laboratory, Skane University Hospital Lund	0	2	0	0	2
New York Genome Center	0	2	0	0	2
OMIM	1	0	0	0	1
GeneDx	0	0	0	1	1
Fulgent Genetics, Fulgent Genetics	0	1	0	0	1

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