ClinVar Miner

Submissions for variant NM_012120.3(CD2AP):c.1275-11dup

dbSNP: rs569215676
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002087024 SCV002320887 benign not provided 2023-08-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507845 SCV002807121 likely benign Focal segmental glomerulosclerosis 3, susceptibility to 2021-08-19 criteria provided, single submitter clinical testing

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