rs747176196, MFN2

N. diseases: 3
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.
Cerebellar atrophy
CUI: C0740279
Disease: Cerebellar atrophy
67 1.000 1 11989329 missense variant C/T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2016 2016
Cerebellar signs
CUI: C0742038
Disease: Cerebellar signs
5 1.000 1 11989329 missense variant C/T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2016 2016
Pyramidal sign
CUI: C0234132
Disease: Pyramidal sign
10 1.000 1 11989329 missense variant C/T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2016 2016