ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.1979-11C>G

gnomAD frequency: 0.00693  dbSNP: rs182705867
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 RCV002077947 SCV002324213 benign Brachyolmia-amelogenesis imperfecta syndrome 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718990 SCV005318457 benign not provided criteria provided, single submitter not provided

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