ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.1859-20T>C

dbSNP: rs2124520321
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001608341 SCV001835068 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003539396 SCV004322096 likely benign RASopathy 2023-08-28 criteria provided, single submitter clinical testing

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