"GeneDx"[submitter] AND "LOC129993109"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 347552	NM_031296.2(RAB33B):c.-205G>C	LOC129993109, RAB33B +1 more	Single nucleotide variant (non-coding transcript variant)	Smith-McCort dysplasia +1 more	GBenign
Select item 347558	NM_031296.3(RAB33B):c.-54C>G	LOC129993109, RAB33B	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign