ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.828+59C>G

gnomAD frequency: 0.32638  dbSNP: rs7559693
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001527199 SCV001738145 benign Autosomal recessive Alport syndrome 2021-06-10 criteria provided, single submitter clinical testing
GeneDx RCV001673112 SCV001888062 benign not provided 2018-06-24 criteria provided, single submitter clinical testing

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