ClinVar Miner

Submissions for variant NM_032951.3(MLXIPL):c.732C>A (p.Asp244Glu)

gnomAD frequency: 0.01886  dbSNP: rs34922362
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 RCV000947021 SCV001093185 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000947021 SCV005272258 benign not provided criteria provided, single submitter not provided

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