rs6937876, ATG5

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.
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.925 0.200 6 106132754 intron variant G/A snv 0.70 0.010 1.000 1 2019 2019
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.925 0.200 6 106132754 intron variant G/A snv 0.70 0.010 1.000 1 2014 2014