ClinVar Miner

Submissions for variant NM_000071.2(CBS):c.844_845insATCCAGGTGGGGCTTTTGCTGGGCTTGAGCCCTGAAGCCGCGCCCTCTGCAGATCATTGGGGTGGATC

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000200688 SCV000249656 benign not specified 2015-05-01 criteria provided, single submitter clinical testing This variant was found in TAADV2-PANCARD,CBS

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