ClinVar Miner

Variants from IntelligeneCG

Location: United States — Primary collection method: clinical testing
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 total
0 0 0 0 13 13

Gene and significance breakdown #

Total genes and gene combinations: 12
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Gene or gene combination benign total
PMS2 2 2
ATM, C11orf65 1 1
BRCA1 1 1
BRCA2 1 1
BRIP1 1 1
MLH1 1 1
MSH6 1 1
NBN 1 1
SDHB 1 1
SLX4 1 1
TP53 1 1

Condition and significance breakdown #

Total conditions: 9
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Condition benign total
Lynch syndrome I 3 3
Familial cancer of breast 2 2
Hereditary nonpolyposis colorectal cancer type 4 2 2
Breast-ovarian cancer, familial 1 1 1
Fanconi anemia, complementation group J 1 1
Fanconi anemia, complementation group P 1 1
Li-Fraumeni syndrome 1 1 1
Microcephaly, normal intelligence and immunodeficiency 1 1
Paraganglioma and gastric stromal sarcoma 1 1

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