ClinVar Miner

Submissions for variant NM_015559.3(SETBP1):c.2673G>A (p.Arg891=)

gnomAD frequency: 0.00001  dbSNP: rs777737690
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002080816 SCV002380774 likely benign not provided 2021-04-15 criteria provided, single submitter clinical testing

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