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
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.860 1.000 8 2009 2019
dbSNP: rs17249754
rs17249754
0.882 0.120 12 89666809 intron variant G/A snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.800 0.929 14 2010 2019
dbSNP: rs11105378
rs11105378
12 89696964 intron variant C/T snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2010 2012
dbSNP: rs2070759
rs2070759
12 89623959 intron variant G/T snv 0.49
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 1.000 2 2010 2016
dbSNP: rs1401982
rs1401982
12 89595822 intron variant G/A snv 0.60
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.710 1.000 2 2013 2018
dbSNP: rs2681492
rs2681492
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.710 1.000 2 2013 2018
dbSNP: rs11105368
rs11105368
12 89680664 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11105364
rs11105364
12 89675499 intron variant T/G snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7297206
rs7297206
12 89625452 intron variant C/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7136259
rs7136259
1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2019 2019