ClinVar Miner

Submissions for variant NM_004897.5(MINPP1):c.933+34T>A

gnomAD frequency: 0.12000  dbSNP: rs41299159
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001684608 SCV001897079 benign not provided 2020-10-21 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 11297621)
Breakthrough Genomics, Breakthrough Genomics RCV001684608 SCV005319821 benign not provided criteria provided, single submitter not provided
OMIM RCV001822968 SCV000025504 pathogenic Thyroid adenoma 2001-04-01 no assertion criteria provided literature only

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