List of variants in gene combination LOC129993110, RAB33B reported as uncertain significance for bone development 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_031296.3(RAB33B):c.201G>A (p.Gly67=)	rs568007401	0.00005
NM_031296.3(RAB33B):c.193A>G (p.Thr65Ala)	rs2111067573

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