Variants in gene TLN2 - 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
0	0	265	28	16	309

Condition and significance breakdown #

Total conditions: 3

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Condition	uncertain significance	likely benign	benign	total
not specified	258	1	0	259
not provided	6	27	16	49
Myoepithelial tumor	1	0	0	1

Submitter and significance breakdown #

Total submitters: 7

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Submitter	uncertain significance	likely benign	benign	total
Ambry Genetics	258	1	0	259
Labcorp Genetics (formerly Invitae), Labcorp	0	10	13	23
CeGaT Center for Human Genetics Tuebingen	2	18	3	23
Breakthrough Genomics, Breakthrough Genomics	0	3	9	12
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	2	0	0	2
Quest Diagnostics Nichols Institute San Juan Capistrano	2	0	0	2
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine	1	0	0	1

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