ClinVar Miner

Submissions for variant NM_001042472.3(ABHD12):c.787+3G>A

gnomAD frequency: 0.00016  dbSNP: rs202150912
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
Eurofins Ntd Llc (ga) RCV000180201 SCV000232595 uncertain significance not provided 2014-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000180201 SCV001721026 benign not provided 2024-01-19 criteria provided, single submitter clinical testing

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