ClinVar Miner

Submissions for variant NM_005918.4(MDH2):c.902A>G (p.Lys301Arg)

gnomAD frequency: 0.03554  dbSNP: rs10256
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674599 SCV001889546 benign not provided 2019-09-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001674599 SCV002361966 benign not provided 2025-02-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001674599 SCV005265521 benign not provided criteria provided, single submitter not provided

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