ClinVar Miner

Submissions for variant NM_005739.4(RASGRP1):c.795C>T (p.Arg265=)

gnomAD frequency: 0.00003  dbSNP: rs572243858
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002647571 SCV003513752 likely benign not provided 2024-10-02 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV003151448 SCV003839944 likely benign not specified 2022-04-28 no assertion criteria provided clinical testing

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