ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.912A>G (p.Ala304=)

dbSNP: rs2134168641
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001452757 SCV001656430 likely benign RASopathy 2020-06-10 criteria provided, single submitter clinical testing

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