ClinVar Miner

Submissions for variant NM_001927.4(DES):c.75= (p.Pro25=)

gnomAD frequency: 0.10153 dbSNP: rs1318299

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	RCV000154433	SCV000204102	benign	not specified	2008-11-16	criteria provided, single submitter	clinical testing

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