ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.*2244_*2245dup

dbSNP: rs3832123
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193464 SCV000249009 likely benign not specified 2015-07-30 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260090 SCV000430345 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000334114 SCV000430346 likely benign Gingival fibromatosis 2016-06-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467656 SCV002763163 likely benign Noonan syndrome 4 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467655 SCV002763164 likely benign Fibromatosis, gingival, 1 criteria provided, single submitter clinical testing

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