List of variants in gene combination LOC129993109, RAB33B reported as uncertain significance for Smith-McCort dysplasia

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_031296.2(RAB33B):c.-363G>A	rs535498698	0.00494
NM_031296.2(RAB33B):c.-167A>C	rs190790812	0.00374
NM_031296.2(RAB33B):c.-193G>T	rs886059075	0.00024
NM_031296.2(RAB33B):c.-342T>C	rs886059073	0.00016
NM_031296.2(RAB33B):c.-163C>T	rs886059076	0.00012
NM_031296.2(RAB33B):c.-255C>T	rs886059074	0.00006
NM_031296.2(RAB33B):c.-160G>A	rs774087744	0.00004
NM_031296.2(RAB33B):c.-348G>C	rs886059072
NM_031296.2(RAB33B):c.-368C>T	rs886059071

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