ClinVar Miner

Submissions for variant NM_005633.3(SOS1):c.487A>G (p.Lys163Glu) (rs886042206)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000329053 SCV000332537 uncertain significance not provided 2015-07-06 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000764408 SCV000895465 uncertain significance Gingival fibromatosis 1; Noonan syndrome 4 2018-10-31 criteria provided, single submitter clinical testing

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