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: rs12067906
rs12067906 		1 192462868 intron variant T/C snv 0.12
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs1223397
rs1223397
TBC1D7 ; PHACTR1 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs17031508
rs17031508
BANK1
4 101639133 intron variant A/C snv 8.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs633185
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2011 2019
dbSNP: rs6749447
rs6749447
STK39
2 168184876 intron variant T/G snv 0.37
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2009 2009
dbSNP: rs7984522
rs7984522
MYO16
13 108695311 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs1004467
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs10143078
rs10143078
COX16 ; SYNJ2BP ; SYNJ2BP-COX16
14 70414772 intron variant A/C snv 6.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs10197121
rs10197121
RRM2
2 10153562 intron variant C/T snv 0.64
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs10444602
rs10444602 		12 131708291 upstream gene variant T/G snv 0.51
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs10555137
rs10555137
CASC8
8 127457345 intron variant C/T snv 6.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11066280
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11099098
rs11099098 		0.925 0.120 4 80248758 intergenic variant G/C;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs11105354
rs11105354
ATP2B1
12 89632746 intron variant A/G snv 0.15
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11160059
rs11160059
SLC24A4
14 92340986 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11222084
rs11222084
ZBTB44-DT
11 130403335 non coding transcript exon variant A/T snv 0.30
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1156725
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11659639
rs11659639 		18 60500379 intron variant T/G snv 1.1E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1173756
rs1173756
NPR3
5 32789746 3 prime UTR variant T/C snv 0.56 0.60
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1173766
rs1173766 		5 32804422 intergenic variant T/C snv 0.57
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1173771
rs1173771 		5 32814922 regulatory region variant A/G snv 0.65
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11816631
rs11816631 		10 97802815 intergenic variant A/G snv 8.8E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs12098903
rs12098903 		11 55899037 downstream gene variant A/T snv 5.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs12098904
rs12098904 		11 55899077 downstream gene variant A/T snv 5.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011