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: rs1275988
rs1275988
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1731243
rs1731243
2 26707543 intron variant C/T snv 0.48
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1731249
rs1731249
2 26697157 intron variant T/A snv 0.48
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs35021474
rs35021474
2 26693976 intron variant C/G snv 0.48
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018