ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.1509T>C (p.Asp503=)

dbSNP: rs2124537148
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002108239 SCV002398786 likely benign RASopathy 2021-06-30 criteria provided, single submitter clinical testing

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