ClinVar Miner

List of variants in gene combination LOC107984036, RAB33B reported as uncertain significance for Smith-McCort dysplasia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_031296.2(RAB33B):c.-160G>A rs774087744
NM_031296.2(RAB33B):c.-163C>T rs886059076
NM_031296.2(RAB33B):c.-167A>C rs190790812
NM_031296.2(RAB33B):c.-193G>T rs886059075
NM_031296.2(RAB33B):c.-255C>T rs886059074
NM_031296.2(RAB33B):c.-342T>C rs886059073
NM_031296.2(RAB33B):c.-348G>C rs886059072
NM_031296.2(RAB33B):c.-363G>A rs535498698
NM_031296.2(RAB33B):c.-368C>T rs886059071

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