ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1210C>G (p.Pro404Ala)

dbSNP: rs748121445
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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 RCV002638000 SCV003516413 likely benign Noonan syndrome 9 2023-10-03 criteria provided, single submitter clinical testing

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