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: rs2681472
rs2681472
0.846 0.036 12 89615182 intron variant A/G snp 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.820 1.000 3 2010 2013
dbSNP: rs17249754
rs17249754
0.878 0.107 12 89666809 intron variant G/A snp 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.790 0.889 10 2010 2016
dbSNP: rs11105368
rs11105368
12 89680664 intron variant G/A,C snp 3.2E-05; 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1 2017 2017
dbSNP: rs11105378
rs11105378
12 89696964 intron variant C/T snp 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2070759
rs2070759
12 89623959 intron variant G/T snp 0.49
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010