ClinVar Miner

Submissions for variant NM_006910.5(RBBP6):c.4668A>G (p.Glu1556=)

gnomAD frequency: 0.00129  dbSNP: rs114113023
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV003151627 SCV003839950 likely benign not specified 2022-07-28 no assertion criteria provided clinical testing

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