Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113296370
rs113296370
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs17030613
rs17030613
1 112648185 intron variant A/C snv 0.19
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs403814
rs403814
18 6282594 intron variant A/C snv 0.27
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.710 1.000 1 2016 2016
dbSNP: rs4387287
rs4387287
10 103918139 5 prime UTR variant A/C snv 0.69
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2016 2016
dbSNP: rs4833103
rs4833103
0.925 0.160 4 38813881 intron variant A/C snv 0.64
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs8098380
rs8098380
18 721563 downstream gene variant A/C snv 0.33
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs2932538
rs2932538
1 112673921 intron variant A/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.810 1.000 1 2011 2013
dbSNP: rs6418
rs6418
8 142914947 intron variant A/C;G snv 0.42
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs7006531
rs7006531
8 94098516 intron variant A/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2017 2017
dbSNP: rs12715461
rs12715461
3 53544856 intron variant A/C;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs1859168
rs1859168
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs2521501
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
dbSNP: rs13333226
rs13333226
0.827 0.200 16 20354332 intron variant A/G snv 0.23
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.810 1.000 2 2010 2016
dbSNP: rs2681472
rs2681472
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.860 1.000 2 2009 2019
dbSNP: rs820430
rs820430
3 27507409 regulatory region variant A/G snv 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.710 1.000 2 2015 2018
dbSNP: rs1004467
rs1004467
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.760 0.857 1 2011 2018
dbSNP: rs10279895
rs10279895
7 27288591 intergenic variant A/G snv 2.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2017 2017
dbSNP: rs11067763
rs11067763
12 115760536 intron variant A/G snv 0.16
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2015 2015
dbSNP: rs11124945
rs11124945
1.000 0.040 2 43650017 intron variant A/G snv 0.21
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs11230728
rs11230728
11 61510226 3 prime UTR variant A/G snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs1173771
rs1173771
5 32814922 regulatory region variant A/G snv 0.65
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs16982520
rs16982520
1.000 0.040 20 59183665 intron variant A/G snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2009 2009
dbSNP: rs2342883
rs2342883
3 14869013 intron variant A/G snv 0.69
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2019 2019
dbSNP: rs35444
rs35444
12 115114632 intergenic variant A/G snv 0.38
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018