Variants studied for Immunodeficiency 83, susceptibility to viral infections

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	3	1	1	9	14

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
TLR3	1	3	1	1	9	14

Submitter and significance breakdown #

Total submitters: 5

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Submitter	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
OMIM	0	0	0	0	9	9
Neuberg Centre For Genomic Medicine, NCGM	0	3	0	0	0	3
Genome Diagnostics Laboratory, University Medical Center Utrecht	0	0	1	0	0	1
Centogene AG - the Rare Disease Company	1	0	0	0	0	1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	0	0	0	1	0	1

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