ClinVar Miner

Variants studied for Pheochromocytoma; Familial medullary thyroid carcinoma

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 total
0 1 0 0 0 1

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic total
RET 1 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely pathogenic total
Clinical Genomics Laboratory, Washington University in St. Louis 1 1

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