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: rs3087894
rs3087894
1 85321435 3 prime UTR variant G/A;C snv 8.0E-06; 0.34
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs480414
rs480414
1.000 0.080 1 85461780 intron variant G/A snv 0.31
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018