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: rs17249754
rs17249754
0.882 0.120 12 89666809 intron variant G/A snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 0.929 3 2010 2019
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: rs167479
rs167479
19 11416089 missense variant T/A;C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 2 2016 2016
dbSNP: rs1902859
rs1902859
4 80236549 regulatory region variant T/C snv 0.27
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 2 2015 2018
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: rs4409766
rs4409766
1.000 0.040 10 102856906 intron variant T/C snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 2 2015 2018
dbSNP: rs633185
rs633185
0.925 0.080 11 100722807 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 2 2011 2018
dbSNP: rs6969780
rs6969780
7 27119517 splice region variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 2 2016 2017
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: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 2 2015 2018
dbSNP: rs10033366
rs10033366
4 110409934 intron variant T/C snv 0.92
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs10069554
rs10069554
5 33204354 intron variant T/C snv 0.45
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs10184428
rs10184428
2 164155317 intron variant C/A;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs1027989
rs1027989
LYN
8 55901862 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2017 2017
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: rs10745332
rs10745332
1 112646431 intron variant G/A snv 0.77
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2015 2015
dbSNP: rs10776752
rs10776752
1 112501706 intron variant G/T snv 8.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs10857147
rs10857147
1.000 0.040 4 80259918 intergenic variant A/T snv 0.25
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs10948071
rs10948071
6 43312975 intron variant C/T snv 0.46
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs11014166
rs11014166
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2009 2009
dbSNP: rs11020821
rs11020821
11 94538497 intergenic variant C/A snv 0.28
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2012 2012
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.710 1.000 1 2014 2015
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: rs11099098
rs11099098
0.925 0.120 4 80248758 intergenic variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018
dbSNP: rs11105364
rs11105364
12 89675499 intron variant T/G snv 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2018 2018