ClinVar Miner

Submissions for variant NM_000789.4(ACE):c.1343-17A>G

gnomAD frequency: 0.00106  dbSNP: rs139287666
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002174827 SCV002347440 benign not provided 2024-12-30 criteria provided, single submitter clinical testing

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