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: rs12576239
rs12576239
1.000 0.080 11 2481089 intron variant C/T snv 0.16
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs199473444
rs199473444
1.000 0.080 11 2445138 missense variant C/T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2237892
rs2237892
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3864884
rs3864884
1.000 0.080 11 2460862 intron variant C/T snv 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017