ClinVar Miner

Submissions for variant NC_000023.11:g.103181775C>G (rs746040794)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine RCV000993783 SCV000995910 benign not specified no assertion criteria provided research This variant was dentified in a patient with an Xq22del, and noted in the context of the Xq22del mechanism of formation, but not believed to be indepdently causative of the observed phenotype.

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