ClinVar Miner

Variants studied for High molecular weight kininogen deficiency

Coded as:
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 affects total
0 0 1 0 0 3 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance affects total
KNG1 1 3 4

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance affects total
OMIM 0 3 3
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 1 0 1

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