rs863223326, LBR

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
HEM dysplasia
CUI: C2931048
Disease: HEM dysplasia
0.700 CausalMutation CLINVAR
Pelger-Huet Anomaly
CUI: C0030779
Disease: Pelger-Huet Anomaly
0.700 CausalMutation CLINVAR