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: rs1057518856
rs1057518856
0.882 0.240 16 2102397 missense variant A/T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 0
dbSNP: rs1057518897
rs1057518897
0.925 0.120 16 2103746 missense variant C/T snv 7.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 0
dbSNP: rs1057518899
rs1057518899
16 2111647 stop gained G/A snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 0
dbSNP: rs1057518959
rs1057518959
16 2091794 missense variant A/G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 0