ClinVar Miner

Submissions for variant NM_144498.4(OSBPL2):c.674+9C>T

gnomAD frequency: 0.00101  dbSNP: rs149348543
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001574281 SCV001801076 likely benign not provided 2020-10-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001574281 SCV002406410 benign not provided 2024-01-11 criteria provided, single submitter clinical testing

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