rs2189480, VDR

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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 1.000 0.040 12 47870045 intron variant G/T snv 0.36 0.010 1.000 1 2019 2019
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 12 47870045 intron variant G/T snv 0.36 0.010 1 2019 2019