rs745607430, NRG1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fahr's syndrome (disorder)
CUI: C0393590
Disease: Fahr's syndrome (disorder)
0.010 GeneticVariation BEFREE Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease). 20838928 2011
Idiopathic basal ganglia calcification 1
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
0.010 GeneticVariation BEFREE Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease). 20838928 2011