Variants from Harris Lab, University of Minnesota

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
0	0	0	0	0	99	99

Gene and significance breakdown #

Total genes and gene combinations: 13

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Gene or gene combination	not provided	total
MRE11	18	18
RAD52	17	17
RAD50	13	13
MLH1	12	12
NBN	12	12
MSH2	9	9
ERCC1	6	6
AICDA	5	5
intergenic	2	2
RAD50, TH2-LCR, TH2LCRR	2	2
APEX1	1	1
LOC107372315	1	1
LOC126861412, RAD52	1	1

Condition and significance breakdown #

Total conditions: 1

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Condition	not provided	total
not provided	99	99

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