ClinVar Miner

Submissions for variant NM_004285.4(H6PD):c.1651C>A (p.Arg551=)

dbSNP: rs760131543
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002086148 SCV002385697 likely benign not provided 2022-10-17 criteria provided, single submitter clinical testing

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