Variants studied for Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection

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	not provided	total
25	3	199	200	15	1	441

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
STAT2	23	3	197	200	15	1	437
IFNAR2, IFNAR2-IL10RB	2	0	0	0	0	0	2
LOC130008075, STAT2	0	0	2	0	0	0	2

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	20	3	197	200	15	0	435
Baylor Genetics	1	0	4	0	0	0	5
OMIM	3	0	0	0	0	0	3
Laboratory of Medical Genetics Unit, Bambino Gesù Children's Hospital	2	0	0	0	0	0	2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	0	0	0	0	1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	1	0	0	0	1
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	1	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	0	1

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