ClinVar Miner

Submissions for variant NM_002168.4(IDH2):c.207+4G>A

gnomAD frequency: 0.00331  dbSNP: rs77995170
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000970557 SCV001118143 benign D-2-hydroxyglutaric aciduria 2 2024-01-24 criteria provided, single submitter clinical testing

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