ClinVar Miner

Submissions for variant NM_001009999.3(KDM1A):c.1072+3A>G (rs1553129313)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000600770 SCV000716363 likely benign not specified 2017-02-24 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
GenomeConnect, ClinGen RCV000845019 SCV000986852 not provided Neurodevelopmental and congenital anomalies no assertion provided phenotyping only Variant interpretted as Uncertain significance and reported on 04/10/2018 by GTR ID Illumina Clinical Services Laboratory. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant.

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