Disease: SMITH-MCCORT DYSPLASIA 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776958
rs587776958
Entrez Id: 83452;107984036
Gene Symbol: RAB33B;LOC107984036
RAB33B;LOC107984036
CUI: C3714896
Disease:
SMITH-MCCORT DYSPLASIA 2 		0.800 GeneticVariation UNIPROT
dbSNP: rs587776958
rs587776958
Entrez Id: 83452;107984036
Gene Symbol: RAB33B;LOC107984036
RAB33B;LOC107984036
CUI: C3714896
Disease:
SMITH-MCCORT DYSPLASIA 2 		C 0.800 CausalMutation CLINVAR