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: rs9969436
rs9969436
8 10985149 intron variant T/G snv 0.58
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9961091
rs9961091
18 787846 intron variant G/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs988398
rs988398
3 169381073 intron variant C/T snv 0.45
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9874923
rs9874923
3 20060071 intron variant C/G;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2013 2013
dbSNP: rs9814480
rs9814480
3 53556438 intron variant C/T snv 0.14
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9810888
rs9810888
3 53601568 intron variant T/G snv 0.51
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9388520
rs9388520
6 126795330 intron variant G/A snv 0.36
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9375463
rs9375463
6 126845743 intron variant A/C;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9313772
rs9313772
5 158377449 intron variant C/T snv 0.30
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2011 2011
dbSNP: rs9303509
rs9303509
17 66534769 intron variant C/A;G snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs9292468
rs9292468
5 32818967 intergenic variant T/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs909116
rs909116
0.925 0.080 11 1920716 intron variant T/C snv 0.44
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs900145
rs900145
11 13272358 upstream gene variant C/T snv 0.62
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2016 2018
dbSNP: rs899366
rs899366
8 11572976 upstream gene variant G/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs893311
rs893311
11 16296972 intron variant G/T snv 0.16
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs891511
rs891511
7 151007755 intron variant G/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs890431
rs890431
17 48609478 intron variant T/A;C snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 3 2016 2018
dbSNP: rs820430
rs820430
3 27507409 regulatory region variant A/G snv 0.30
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs8098380
rs8098380
18 721563 downstream gene variant A/C snv 0.33
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs8068318
rs8068318
17 61406405 non coding transcript exon variant C/T snv 0.56
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs79581935
rs79581935
5 174811890 intron variant A/T snv 6.5E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7953257
rs7953257
12 112246417 intron variant A/G;T snv 0.71
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7940807
rs7940807
11 16892459 intron variant G/T snv 0.21
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7928655
rs7928655
11 13278705 intron variant C/G snv 0.61
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018