rs745607430, NRG1

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Fahr's syndrome (disorder)
CUI: C0393590
Disease: Fahr's syndrome (disorder)
3 0.925 0.120 8 32764088 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.010 1.000 1 2011 2011
Idiopathic basal ganglia calcification 1
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
26 0.925 0.120 8 32764088 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.010 1.000 1 2011 2011