ClinVar Miner

Submissions for variant NM_001482.3(GATM):c.1159+19A>T

dbSNP: rs187979088
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001536783 SCV001753590 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002071928 SCV002344481 benign Arginine:glycine amidinotransferase deficiency 2024-12-08 criteria provided, single submitter clinical testing

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