ClinVar Miner

Submissions for variant NC_000006.12:g.32853751C>G

gnomAD frequency: 0.00013  dbSNP: rs760815768
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 RCV001467138 SCV001671157 likely benign MHC class I deficiency 2023-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707393 SCV005225661 likely benign not provided criteria provided, single submitter not provided

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