ClinVar Miner

Submissions for variant NM_001318510.2(ACSL4):c.1561G>A (p.Asp521Asn) (rs1556225792)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000622725 SCV000740725 uncertain significance Inborn genetic diseases 2014-08-14 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: UNCERTAIN: Alteration(s) of Uncertain Clinical Significance Detected
Fulgent Genetics,Fulgent Genetics RCV000764856 SCV000896012 uncertain significance Mental retardation 63, X-linked 2018-10-31 criteria provided, single submitter clinical testing

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