rs12155400, HDAC9

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 7 18389298 intron variant A/G snv 2.9E-02 0.010 1.000 1 2013 2013
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 7 18389298 intron variant A/G snv 2.9E-02 0.010 1.000 1 2013 2013