ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1861T>G (p.Phe621Val) (rs1555370029)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000585616 SCV000692788 uncertain significance not provided 2017-10-31 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000765167 SCV000896397 uncertain significance Noonan syndrome 9 2018-10-31 criteria provided, single submitter clinical testing

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