ClinVar Miner

Submissions for variant NM_004208.4(AIFM1):c.1113C>T (p.Ser371=) (rs724160027)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000904868 SCV001049418 likely benign not provided 2018-04-25 criteria provided, single submitter clinical testing
Deafness Gene Diagnosis,Xijing Hospital RCV000149871 SCV000196725 likely benign Deafness, X-linked 5 no assertion criteria provided clinical testing

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