Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs13405173
PDE1A
2 182449087 intron variant A/C snv 8.8E-03 3
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs9375463 6 126845743 intron variant A/C;T snv 3
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs10897164
LRRC10B
11 61510303 3 prime UTR variant A/G snv 0.13 3
rs11191871
LOC102724351
10 103947673 intergenic variant A/G snv 5.2E-02 2
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs12118370
ST7L
1 112605645 intron variant A/G snv 0.24 3
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs16833934 3 164019462 intergenic variant A/G snv 0.34 2
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2048765
HDAC4
2 239286459 intron variant A/G snv 9.6E-02 2
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs284844
WBP1L
10 102794772 intron variant A/G snv 0.82 3