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: rs137852704
rs137852704
0.882 0.160 16 23380574 stop gained C/G;T snv 4.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs149868979
rs149868979
1.000 0.120 16 23380566 missense variant G/A snv 1.5E-04 1.5E-04
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2011 2017
dbSNP: rs1799979
rs1799979
1.000 0.040 16 23380659 missense variant C/G;T snv 8.1E-06; 2.1E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2004 2004
dbSNP: rs1799980
rs1799980
16 23377219 missense variant G/T snv 9.8E-03 3.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3743966
rs3743966
1.000 0.040 16 23380309 intron variant A/T snv 0.23
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014