ClinVar Miner

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

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_031296.3(RAB33B):c.*1303C>T rs4074940
NM_031296.3(RAB33B):c.*2651C>A rs3088313
NM_031296.3(RAB33B):c.-54C>G rs13128486

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