ClinVar Miner

Variants in gene MUC5B

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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 not provided total
0 0 7 34 102 1 1 143

Condition and significance breakdown #

Total conditions: 4
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Condition uncertain significance likely benign benign risk factor not provided total
not specified 6 34 102 0 0 141
Idiopathic fibrosing alveolitis, chronic form 0 0 0 0 1 1
Pulmonary fibrosis, idiopathic, susceptibility to 0 0 0 1 0 1
not provided 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance likely benign benign risk factor not provided total
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 6 33 101 0 1 141
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 1 1 4 0 0 6
OMIM 0 0 0 1 0 1

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