ClinVar Miner

Submissions for variant NM_201525.4(ADGRG1):c.1146G>A (p.Leu382=)

gnomAD frequency: 0.00003  dbSNP: rs770806177
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 RCV000980889 SCV001128849 likely benign not provided 2024-03-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276426 SCV001462699 likely benign Bilateral frontoparietal polymicrogyria 2020-06-09 no assertion criteria provided clinical testing

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