List of variants in gene combination LOC112997583, SQSTM1 reported as benign for bone remodeling 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: 1

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HGVS	dbSNP	gnomAD frequency
NM_003900.5(SQSTM1):c.*279C>G	rs11548631	0.01439

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