ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.828+20A>G (rs13386404)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000241777 SCV000302087 benign not specified criteria provided, single submitter clinical testing
Invitae RCV001513335 SCV001720935 benign not provided 2020-11-23 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001527198 SCV001738144 benign Alport syndrome, autosomal recessive 2021-06-10 criteria provided, single submitter clinical testing
GeneDx RCV001513335 SCV001838068 benign not provided 2018-06-21 criteria provided, single submitter clinical testing

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