Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25