ClinVar Miner

Variants studied for Budd-Chiari syndrome

Included ClinVar conditions (3):
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
1 0 153 18 42 214

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic uncertain significance likely benign benign total
F5 0 144 17 41 202
INSL6, JAK2 1 8 1 1 11
JAK2, LOC130001497 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 152 14 40 206
Fulgent Genetics, Fulgent Genetics 1 2 5 2 10

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