LBR, lamin B receptor, 3930

N. diseases: 307; N. variants: 17
Disease: Reynolds syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200180113
rs200180113
Entrez Id: 3930
Gene Symbol: LBR
LBR
CUI: C0748397
Disease:
Reynolds syndrome 		0.800 GeneticVariation UNIPROT
dbSNP: rs200180113
rs200180113
Entrez Id: 3930
Gene Symbol: LBR
LBR
CUI: C0748397
Disease:
Reynolds syndrome 		A 0.800 CausalMutation CLINVAR
dbSNP: rs200180113
rs200180113
Entrez Id: 3930
Gene Symbol: LBR
LBR
CUI: C0748397
Disease:
Reynolds syndrome 		A 0.800 GeneticVariation CLINVAR