ClinVar Miner

Submissions for variant NM_005896.4(IDH1):c.211G>A (p.Val71Ile)

gnomAD frequency: 0.01337  dbSNP: rs73070954
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000962004 SCV001109065 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000962004 SCV005240878 benign not provided criteria provided, single submitter not provided
ITMI RCV000121203 SCV000085374 not provided not specified 2013-09-19 no assertion provided reference population

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