rs17127024, JAK1

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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.925 0.280 1 64837448 intron variant G/T snv 5.1E-02 0.010 1.000 1 2014 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.925 0.280 1 64837448 intron variant G/T snv 5.1E-02 0.010 1.000 1 2012 2012