ClinVar Miner

Submissions for variant NM_201525.4(ADGRG1):c.1560C>T (p.Phe520=)

gnomAD frequency: 0.00001  dbSNP: rs548451753
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001467739 SCV001671768 likely benign not provided 2023-10-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826296 SCV002089407 likely benign Bilateral frontoparietal polymicrogyria 2021-07-15 no assertion criteria provided clinical testing

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