ClinVar Miner

Submissions for variant NM_053274.3(GLMN):c.978-4T>C (rs750401776)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV000351035 SCV000840218 not provided Glomuvenous malformations no assertion provided phenotyping only GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.
Illumina Clinical Services Laboratory,Illumina RCV000351035 SCV000359059 uncertain significance Glomuvenous malformations 2016-06-14 criteria provided, single submitter clinical testing

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