ClinVar Miner

Submissions for variant NM_139159.5(DPP9):c.1696G>A (p.Glu566Lys)

gnomAD frequency: 0.00219  dbSNP: rs200229921
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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
Labcorp Genetics (formerly Invitae), Labcorp RCV000890585 SCV001034340 benign not provided 2018-07-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000890585 SCV004146312 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing DPP9: BS2
Breakthrough Genomics, Breakthrough Genomics RCV000890585 SCV005309623 benign not provided criteria provided, single submitter not provided

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