ClinVar Miner

Submissions for variant NM_005215.4(DCC):c.1667del (p.Gly556fs)

dbSNP: rs1568364038
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Personalized Medicine, Children's Hospital Los Angeles RCV000735410 SCV000854530 likely pathogenic Bone marrow hypocellularity criteria provided, single submitter clinical testing

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