Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs197922
rs197922
0.925 0.080 17 46931204 missense variant G/A snv 0.35 0.33
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3785889
rs3785889
0.827 0.080 17 46928464 intron variant G/A snv 0.45
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2013 2013