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: rs10509681
rs10509681
0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs11572080
rs11572080
0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2005 2005