ClinVar Miner

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

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_031296.3(RAB33B):c.*1077G>A rs115582784
NM_031296.3(RAB33B):c.*1403C>A rs75661332
NM_031296.3(RAB33B):c.*2026G>A rs144602972
NM_031296.3(RAB33B):c.*254A>G rs78192594
NM_031296.3(RAB33B):c.*543C>T rs79952078
NM_031296.3(RAB33B):c.*590T>C rs78607198
NM_031296.3(RAB33B):c.*595G>A rs13137997
NM_031296.3(RAB33B):c.-36C>T rs182647425

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