Disease: Systolic Pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 5
rs17037390
MTHFR
1.000 0.040 1 11800786 non coding transcript exon variant G/A snv 0.18 3
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 6
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2071382
FES
1.000 0.040 15 90884967 intron variant T/C snv 0.57 2
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs2327429
TARID ; TCF21
0.882 0.120 6 133888699 non coding transcript exon variant T/C snv 0.24 2
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs34991912
FGD5
1.000 0.040 3 14884844 intron variant T/A;C snv 2
rs3745348
MYO9B
1.000 0.040 19 17101600 intron variant C/T snv 0.38 2
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs7500448
CDH13
1.000 0.040 16 83012185 intron variant A/G snv 0.20 3