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: rs9349379
rs9349379
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2018 2019
dbSNP: rs2026458
rs2026458
0.882 0.080 6 12825642 intron variant C/T snv 0.34
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016