Disease: Systolic blood pressure measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92