ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.468+5ATTTT[2] (rs3832900)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000253670 SCV000308127 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000272078 SCV000382544 benign Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000329499 SCV000382545 benign Brain small vessel disease with hemorrhage 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000386441 SCV000382546 benign Acquired porencephaly 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000329499 SCV000677162 benign Brain small vessel disease with hemorrhage 2017-06-01 criteria provided, single submitter clinical testing

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