Variants studied for Watson syndrome

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
39	12	250	106	30	11	443

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
NF1	38	12	230	104	30	11	420
LOC111811965, MIR4733HG, NF1	1	0	20	2	0	0	23

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	31	12	142	84	0	0	269
Illumina Laboratory Services, Illumina	0	0	107	24	29	0	160
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	6	0	4	0	1	0	11
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	10	10
OMIM	3	0	0	0	0	0	3
New York Genome Center	1	0	2	0	0	0	3
Baylor Genetics	0	0	2	0	0	0	2
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	1	0	0	0	0	0	1
Molecular Genetics Lab, CHRU Brest	1	0	0	0	0	0	1
Pediatric Genetics Clinic, Sheba Medical Center	1	0	0	0	0	0	1
GenomeConnect - Brain Gene Registry	0	0	0	0	0	1	1

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