ClinVar Miner

Submissions for variant NM_017857.4(SSH3):c.1383_1384dup (p.Ile462fs)

dbSNP: rs773711729
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenomeConnect, ClinGen RCV000845100 SCV000986952 not provided not provided no assertion provided phenotyping only Variant interpretted as uncertain significance and reported on 07/06/2015 by GTR ID 1006. 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.

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