ClinVar Miner

Submissions for variant NM_198291.3(SRC):c.582C>T (p.Phe194=)

gnomAD frequency: 0.00001  dbSNP: rs766810850
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001819601 SCV002072379 likely benign not specified 2019-04-05 criteria provided, single submitter clinical testing

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