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: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2016 2017
dbSNP: rs1128503
rs1128503
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs17327624
rs17327624
7 87587501 intron variant G/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3789243
rs3789243
0.776 0.120 7 87591570 intron variant A/G snv 0.50
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4148734
rs4148734
7 87564281 intron variant G/A snv 0.22
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016