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: rs3743966
rs3743966
1.000 0.040 16 23380309 intron variant A/T snv 0.23
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs889299
rs889299
1.000 0.040 16 23370593 intron variant G/A snv 0.25
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2008 2008