ClinVar Miner

Submissions for variant NM_000075.4(CDK4):c.600T>G (p.Val200=)

dbSNP: rs2140385676
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001446430 SCV001649476 likely benign Familial melanoma 2020-04-11 criteria provided, single submitter clinical testing

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