ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.424-98=

gnomAD frequency: 0.17991  dbSNP: rs7163339
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
GeneReviews RCV000034275 SCV000058215 benign Legius syndrome 2010-10-14 no assertion criteria provided curation Converted during submission to Benign.

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