ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.*634_*635AT[8] (rs886049952)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000371728 SCV000382274 uncertain significance Acquired porencephaly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000268022 SCV000382275 uncertain significance Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000323137 SCV000382276 uncertain significance Brain small vessel disease with hemorrhage 2016-06-14 criteria provided, single submitter clinical testing

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