ClinVar Miner

Variants studied for acquired polycythemia vera

Included ClinVar conditions (4):
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 not provided total
2 1 2 1 1 2 8

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
INSL6, JAK2 1 0 2 1 1 2 6
ATM 1 0 0 0 0 0 1
JAK1, LOC126805749 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Fulgent Genetics, Fulgent Genetics 1 0 1 1 1 0 4
Database of Curated Mutations (DoCM) 0 1 0 0 0 1 2
OMIM 1 0 0 0 0 0 1
Baylor Genetics 0 0 1 0 0 0 1
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 1 0 0 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 0 1 0 0 0 1
GenomeConnect, ClinGen 0 0 0 0 0 1 1
University Health Network, Princess Margaret Cancer Centre 1 0 0 0 0 0 1
Provincial Medical Genetics Program of British Columbia, University of British Columbia 1 0 0 0 0 0 1
Molecular Diagnostics Laboratory, University of Rochester Medical Center 1 0 0 0 0 0 1

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