ClinVar Miner

Submissions for variant NM_015559.3(SETBP1):c.1879C>T (p.Arg627Cys)

gnomAD frequency: 0.00602  dbSNP: rs146193261
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000870942 SCV001012519 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000870942 SCV001145530 benign not provided 2019-07-01 criteria provided, single submitter clinical testing
GeneDx RCV000870942 SCV001752236 benign not provided 2018-10-21 criteria provided, single submitter clinical testing

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