ClinVar Miner

Submissions for variant NM_006270.5(RRAS):c.495C>T (p.His165=)

gnomAD frequency: 0.00005  dbSNP: rs765681955
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001475069 SCV001679252 likely benign Noonan syndrome 2020-08-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003426131 SCV004140440 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing RRAS: BP4, BP7

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