Source: GWASDB

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: 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 1 2009 2019
dbSNP: rs1799945
rs1799945
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.840 1.000 1 2011 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 1 2010 2016
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: rs4373814
rs4373814
10 18131043 intergenic variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.810 1.000 1 2011 2013
dbSNP: rs6596140
rs6596140
5 133686160 intergenic variant C/T snv 0.34
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.810 1.000 1 2012 2012
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: 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: rs11953630
rs11953630
5 158418394 intergenic variant C/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
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: 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: rs2820037
rs2820037
1.000 0.040 1 239273242 intergenic variant A/T snv 0.21
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2007 2007
dbSNP: rs6015450
rs6015450
20 59176062 intron variant A/G snv 0.14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
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 1 2011 2018
dbSNP: rs805303
rs805303
0.925 0.160 6 31648589 intron variant G/A snv 0.45
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
dbSNP: rs932764
rs932764
10 94136183 intron variant A/G snv 0.38
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.800 1.000 1 2011 2011
dbSNP: rs9791170
rs9791170
5 132233934 intron variant T/C snv 0.59
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.710 1.000 1 2009 2009
dbSNP: rs10188442
rs10188442
2 132431666 intron variant C/T snv 0.22
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs10496288
rs10496288
2 83065441 intergenic variant T/C snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs10496289
rs10496289
2 83066256 intergenic variant C/T snv 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs10785581
rs10785581
12 45537190 intron variant C/A;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs12522034
rs12522034
5 36425491 intergenic variant G/A;C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs13353058
rs13353058
10 122991206 3 prime UTR variant A/G snv 7.7E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2010 2010
dbSNP: rs13420028
rs13420028
2 132430533 intron variant T/G snv 0.22
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011