Variants studied for Atypical hemolytic-uremic syndrome with thrombomodulin anomaly

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
0	1	39	6	38	3	85

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
THBD	1	39	6	38	3	85

Submitter and significance breakdown #

Total submitters: 7

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Submitter	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
Illumina Laboratory Services, Illumina	0	34	6	38	0	78
OMIM	0	0	0	0	3	3
Clinical Genomics Laboratory, Washington University in St. Louis	0	2	0	0	0	2
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1
Arcensus	1	0	0	0	0	1
MVZ Medizinische Genetik Mainz	0	1	0	0	0	1

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