ClinVar Miner

Submissions for variant NM_001448.3(GPC4):c.320-15del

dbSNP: rs57898529
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001667754 SCV001887013 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495999 SCV002802224 benign Keipert syndrome; Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2021-08-11 criteria provided, single submitter clinical testing

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