ClinVar Miner

Submissions for variant NM_018127.7(ELAC2):c.1305-8delinsCTCTC

dbSNP: rs1064794813
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722398 SCV000569999 likely benign not provided 2021-03-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002475936 SCV002799037 benign Prostate cancer, hereditary, 2; Combined oxidative phosphorylation defect type 17 2021-07-08 criteria provided, single submitter clinical testing

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