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: rs4149601
rs4149601
0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2008 2009
dbSNP: rs2288775
rs2288775
1.000 0.040 18 58316132 intron variant A/G snv 0.25
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3865418
rs3865418
1.000 0.040 18 58336932 intron variant T/C snv 0.49
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs767730323
rs767730323
18 58351025 missense variant G/A snv 9.1E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017