ClinVar Miner

Variants studied for congenital fibrinogen deficiency

Included ClinVar conditions (2):
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
18 0 47 20 10 95

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic uncertain significance likely benign benign total
FGB 7 26 13 6 52
FGA 6 12 5 3 26
FGG 5 8 2 1 16
FGG, LOC114827822 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 47 20 10 77
OMIM 14 0 0 0 14
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 2 0 0 0 2
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 1 0 0 0 1
Knight Diagnostic Laboratories,Oregon Health and Sciences University 1 0 0 0 1

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