ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2268T>G (p.Pro756=)

dbSNP: rs1555369534
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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 RCV001431860 SCV001634621 likely benign Noonan syndrome 9 2022-10-11 criteria provided, single submitter clinical testing

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