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: rs16849225
rs16849225
2 164050310 intron variant C/T snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2011 2018
dbSNP: rs419076
rs419076
3 169383098 intron variant T/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2011 2018
dbSNP: rs6015450
rs6015450
20 59176062 intron variant A/G snv 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2011 2018
dbSNP: rs932764
rs932764
10 94136183 intron variant A/G snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2011 2017
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2011 2015
dbSNP: rs1173766
rs1173766
5 32804422 intergenic variant T/C snv 0.57
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2011 2018
dbSNP: rs2932538
rs2932538
1 112673921 intron variant A/C;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2011 2017
dbSNP: rs7129220
rs7129220
11 10328991 intron variant G/A snv 0.10
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2011 2017
dbSNP: rs4373814
rs4373814
10 18131043 intergenic variant G/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2011 2011
dbSNP: rs6825911
rs6825911
4 110460482 intron variant C/T snv 0.68
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2011 2011
dbSNP: rs805303
rs805303
0.925 0.160 6 31648589 intron variant G/A snv 0.45
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2011 2011
dbSNP: rs17080102
rs17080102
6 150683634 5 prime UTR variant G/C snv 8.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 6 2013 2019
dbSNP: rs13209747
rs13209747
6 126794309 intron variant C/G;T snv 0.36
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2013 2018
dbSNP: rs17428471
rs17428471
7 27298248 intergenic variant G/T snv 9.4E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2013 2017
dbSNP: rs10826334
rs10826334
10 59620724 intron variant C/A;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs10832417
rs10832417
11 2631427 non coding transcript exon variant T/G snv 0.32
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs10841530
rs10841530
12 20446178 intron variant A/G snv 0.30
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs11693319
rs11693319
2 178873542 3 prime UTR variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs13178964
rs13178964
5 105011948 intron variant A/G snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs1401454
rs1401454
11 16228637 intron variant C/A;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs1669539
rs1669539
1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs16890334
rs16890334
6 78846449 intergenic variant T/C snv 1.9E-03
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs16963349
rs16963349
16 84304628 intron variant T/C snv 7.4E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs2410182
rs2410182
21 39808149 intergenic variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013
dbSNP: rs2735413
rs2735413
16 78019746 intron variant A/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2013 2013