List of variants in gene SMC3 reported as likely benign for De Lange syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005445.3(SMC3):c.-135G>A	rs17127559	0.00003
NM_005445.3(SMC3):c.-130G>A	rs559499419	0.00002
NM_005445.4(SMC3):c.548-5_548-4dup	rs199906378

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