List of variants in gene RAB33B reported as benign for Smith-McCort dysplasia 2

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_031296.3(RAB33B):c.*2651C>A	rs3088313	0.26120
NM_031296.3(RAB33B):c.*1303C>T	rs4074940	0.19380
NM_031296.3(RAB33B):c.-36C>T	rs182647425	0.00916
NM_031296.3(RAB33B):c.*1077G>A	rs115582784	0.00878
NM_031296.3(RAB33B):c.258A>G (p.Leu86=)	rs189262252	0.00016

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