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: rs2276047
rs2276047
1.000 0.040 11 72230337 intron variant A/G snv 0.28 0.33
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs9886
rs9886
11 72238621 3 prime UTR variant G/C snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2007 2007