rs876493, PNMT

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.
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.925 0.160 17 39668292 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.925 0.160 17 39668292 intron variant G/A snv 0.47 0.010 1.000 1 2011 2011