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: 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
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
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
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
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
13 108695311 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.800 1.000 1 2012 2012
dbSNP: rs11168245
rs11168245
1.000 0.040 12 47810716 intron variant C/G snv 0.16
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs11771259
rs11771259
1.000 0.040 7 7237584 intron variant C/G snv 1.0E-01
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs11823543
rs11823543
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs11825181
rs11825181
11 116755542 intron variant G/A snv 0.10
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs12627514
rs12627514
1.000 0.040 21 43339560 intergenic variant C/A;G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs12759054
rs12759054
1.000 0.040 1 233984064 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs13040716
rs13040716
1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs15285
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1549306
rs1549306
1.000 0.040 16 75381443 intron variant T/C snv 0.52
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs200528
rs200528
1.000 0.040 16 24747810 intron variant A/G snv 0.82
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs229340
rs229340
1.000 0.040 21 43535523 intron variant T/C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs2293947
rs2293947
1.000 0.040 3 128378653 intron variant A/C snv 8.4E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs261316
rs261316
15 58341621 intron variant C/T snv 0.57
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2017 2017
dbSNP: rs2869966
rs2869966
1.000 0.040 4 88947927 intron variant C/T snv 0.47
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs2954033
rs2954033
8 125481504 intron variant A/G snv 0.76
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs301819
rs301819
0.882 0.120 1 8441726 intron variant A/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs305221
rs305221
1.000 0.040 1 88733302 intron variant G/A snv 0.59
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs36044436
rs36044436
1.000 0.040 7 74675495 intron variant C/A;G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019