ClinVar Miner

Submissions for variant NC_000006.12:g.32853758G>A

gnomAD frequency: 0.00001  dbSNP: rs868484039
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001931239 SCV002204860 uncertain significance MHC class I deficiency 2021-08-31 criteria provided, single submitter clinical testing

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