Variants studied for Susceptibility to mononeuropathy of the median nerve, mild

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
2	1	311	97	125	535

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	total
SH3TC2	2	1	298	94	119	513
LOC126807546, SH3TC2	0	0	11	3	6	20
LOC114004390, SH3TC2	0	0	2	0	0	2

Submitter and significance breakdown #

Total submitters: 6

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	310	97	125	532
Genome-Nilou Lab	0	0	0	0	5	5
OMIM	2	0	0	0	0	2
Knight Diagnostic Laboratories, Oregon Health and Sciences University	1	1	0	0	0	2
MGZ Medical Genetics Center	0	0	1	0	0	1
DASA	1	0	0	0	0	1

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