ClinVar Miner

Submissions for variant NM_012120.3(CD2AP):c.1516A>G (p.Asn506Asp)

dbSNP: rs1582617802
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000786942 SCV002806904 uncertain significance Focal segmental glomerulosclerosis 3, susceptibility to 2022-01-10 criteria provided, single submitter clinical testing
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000786942 SCV000925846 uncertain significance Focal segmental glomerulosclerosis 3, susceptibility to 2019-02-05 no assertion criteria provided clinical testing

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