ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.87+15G>C

gnomAD frequency: 0.00018  dbSNP: rs375493196
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714937 SCV001938911 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073325 SCV002372287 likely benign RASopathy 2024-01-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002468287 SCV002763614 benign Noonan syndrome 4 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002468286 SCV002763615 benign Fibromatosis, gingival, 1 criteria provided, single submitter clinical testing

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