ClinVar Miner

Submissions for variant NM_033641.4(COL4A6):c.2132-6G>A

dbSNP: rs201589060
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246547 SCV000308137 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000945369 SCV001091374 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002270137 SCV002553270 benign Hearing loss, X-linked 6 2022-03-15 criteria provided, single submitter clinical testing

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