ClinVar Miner

Variants studied for Thrombophilia due to activated protein C resistance

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 risk factor total
4 0 85 50 0 1 139

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign risk factor total
F5 4 85 50 1 139

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic uncertain significance likely benign risk factor total
Illumina Clinical Services Laboratory,Illumina 0 85 50 0 135
OMIM 3 0 0 0 3
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine 0 0 0 1 1
Knight Diagnostic Laboratories,Oregon Health and Sciences University 1 0 0 0 1

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