ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.2792-50dup

dbSNP: rs869215095
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247446 SCV000311196 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001089763 SCV001830428 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467699 SCV002763264 benign Noonan syndrome 4 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467698 SCV002763265 benign Fibromatosis, gingival, 1 criteria provided, single submitter clinical testing
GenomeConnect - CFC International RCV001089763 SCV001245259 not provided not provided no assertion provided phenotyping only Variant interpreted as Benign and reported on 04-30-2009 by Lab or GTR ID 239772. GenomeConnect-CFC International assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. Registry team members make no attempt to reinterpret the clinical significance of the variant.

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