rs1403543, AGTR2

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 X 116170939 intron variant G/A snv 0.48 0.010 1.000 1 2017 2017
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 1.000 0.040 X 116170939 intron variant G/A snv 0.48 0.010 1.000 1 2011 2011