Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4673
rs4673
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2014 2014
dbSNP: rs7195830
rs7195830
0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2016 2016