ClinVar Miner

Submissions for variant NM_012210.4(TRIM32):c.-81-98G>A

gnomAD frequency: 0.04415  dbSNP: rs73515229
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000833751 SCV000975515 benign not provided 2018-06-16 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Breakthrough Genomics, Breakthrough Genomics RCV000833751 SCV005323562 benign not provided criteria provided, single submitter not provided

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