List of variants in gene SMOC2 reported as uncertain significance for tooth hard tissue disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001166412.2(SMOC2):c.400G>A (p.Val134Ile)	rs373406001	0.00006
NM_001166412.2(SMOC2):c.842G>A (p.Cys281Tyr)	rs2115203587

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