ClinVar Miner

Submissions for variant NM_001395002.1(MAP4K4):c.2639+174A>G

dbSNP: rs112366063
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001636308 SCV001851390 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001636308 SCV005246393 benign not provided criteria provided, single submitter not provided

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