ClinVar Miner

Variants studied for Behcet disease

Included ClinVar conditions (1):
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 association total
17 0 0 0 0 5 22

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination pathogenic association total
ADA2 4 0 4
NOD2 4 0 4
IL18R1 0 3 3
MEFV 3 0 3
PSTPIP1 3 0 3
TNFRSF1A 3 0 3
CDK6 0 2 2

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic association total
Department of Immunology, Hospital Universitario Virgen del Rocio 17 0 17
Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, The First Affiliated Hospital of Chongqing Medical University 0 5 5

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