ClinVar Miner

Submissions for variant NM_001846.4(COL4A2):c.862-41G>A

dbSNP: rs7984100
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001588028 SCV001822151 benign Porencephaly 2 2021-07-22 criteria provided, single submitter clinical testing
GeneDx RCV001707912 SCV001935390 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707912 SCV005229205 benign not provided criteria provided, single submitter not provided

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