ClinVar Miner

Submissions for variant NM_031935.3(HMCN1):c.14266+19_14266+22del

dbSNP: rs770465309
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002177771 SCV002347740 likely benign not provided 2022-01-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494070 SCV002802602 likely benign Age related macular degeneration 1 2022-05-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002494070 SCV004172438 likely benign Age related macular degeneration 1 2023-04-11 criteria provided, single submitter clinical testing

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