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: rs30187
rs30187
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2006 2019
dbSNP: rs10050860
rs10050860
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2927615
rs2927615
5 96862499 intron variant G/A snv 0.18
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs469783
rs469783
5 96785820 synonymous variant C/T snv 0.55 0.56
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018