ClinVar Miner

Variants from Harris Lab, University of Minnesota

Location: United States — Primary collection method: not provided
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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 18 18
RAD50 13 13
MLH1 12 12
NBN 11 11
MSH2 9 9
ERCC1 6 6
AICDA 5 5
​intergenic 2 2
RAD50, TH2-LCR, TH2LCRR 2 2
APEX1 1 1
LOC107372315 1 1
NBN, OSGIN2 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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