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: rs2296545
rs2296545
0.851 0.160 10 88583080 missense variant C/G;T snv 0.46
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.050 0.800 5 2011 2016
dbSNP: rs2576178
rs2576178
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.040 0.750 4 2012 2016
dbSNP: rs10887800
rs10887800
0.790 0.280 10 88316086 intron variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2013 2019