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: rs3096277
rs3096277
CDH13 ; LOC105371366
16 83730599 intron variant T/C snv 0.74
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2007 2007
dbSNP: rs7591163
rs7591163 		2 227850659 intergenic variant C/A;G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2007 2007
dbSNP: rs4977950
rs4977950 		9 24732484 intergenic variant G/C;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2009 2009
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: rs13306560
rs13306560
CLCN6 ; MTHFR
1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2010 2010
dbSNP: rs2797221
rs2797221
USH2A
1 215739300 intron variant T/C snv 0.88
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2010 2010
dbSNP: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 3 2011 2011
dbSNP: rs17249754
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 3 2011 2013
dbSNP: rs11191593
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2013
dbSNP: rs1378942
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs1421811
rs1421811
NPR3
5 32714164 intron variant C/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2014
dbSNP: rs1530440
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs16948048
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs16998073
rs16998073 		0.925 0.120 4 80263187 upstream gene variant A/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs17367504
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs2681472
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs2681492
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2013
dbSNP: rs3824755
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2013
dbSNP: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
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: 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