List of variants in gene RAB33B reported as likely benign for bone disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_031296.3(RAB33B):c.*595G>A	rs13137997	0.13673
NM_031296.3(RAB33B):c.*543C>T	rs79952078	0.09274
NM_031296.3(RAB33B):c.*254A>G	rs78192594	0.03930
NM_031296.3(RAB33B):c.*590T>C	rs78607198	0.01799
NM_031296.3(RAB33B):c.*2026G>A	rs144602972	0.01770
NM_031296.3(RAB33B):c.*1403C>A	rs75661332	0.01524
NM_031296.3(RAB33B):c.*1751G>T	rs114169513	0.00234
NM_031296.3(RAB33B):c.*513C>T	rs4131797	0.00158
NM_031296.3(RAB33B):c.*576T>C	rs4131798	0.00144
NM_031296.3(RAB33B):c.677C>T (p.Thr226Met)	rs139823051	0.00099
NM_031296.3(RAB33B):c.*2722T>G	rs539470441	0.00046
NM_031296.3(RAB33B):c.*2548T>G	rs529499632

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