ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.234+8C>T (rs9521650)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000375383 SCV000677153 benign Brain small vessel disease with hemorrhage 2017-06-01 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000177133 SCV000228963 benign not specified 2014-10-21 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000318401 SCV000382568 benign Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375383 SCV000382569 benign Brain small vessel disease with hemorrhage 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000283020 SCV000382570 benign Porencephalic cyst 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000177133 SCV000308116 benign not specified criteria provided, single submitter clinical testing

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