ClinVar Miner

Variants from Breast Care Center, Daerim St. Mary`s Hospital

Location: Korea, Republic of  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
3 3 2 0 0 8

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
BRCA2 0 1 2 3
BRCA1, LOC126862571 0 1 0 1
BRIP1 1 0 0 1
CHEK2 0 1 0 1
SDHA 1 0 0 1
TP53 1 0 0 1

Condition and significance breakdown #

Total conditions: 3
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Condition pathogenic likely pathogenic uncertain significance total
Hereditary cancer-predisposing syndrome 2 2 0 4
Hereditary breast ovarian cancer syndrome 0 1 2 3
Li-Fraumeni syndrome; Hereditary cancer-predisposing syndrome 1 0 0 1

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