ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.258A>G (p.Val86=)

gnomAD frequency: 0.00091  dbSNP: rs142443276
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) RCV000177058 SCV000228875 uncertain significance not provided 2018-06-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000177058 SCV004254287 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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