ClinVar Miner

Submissions for variant NM_001482.3(GATM):c.69+8C>G

dbSNP: rs1044785525
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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 RCV001445180 SCV001648202 likely benign Arginine:glycine amidinotransferase deficiency 2020-08-10 criteria provided, single submitter clinical testing

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