Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs10504249
LINC01602 ; LOC105375856
8 57876522 intron variant A/G snv 1.7E-02 3
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 4
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs1105955 6 126826023 intron variant T/A snv 0.44 3
rs1105956 6 126825734 intron variant G/A snv 0.44 2
rs11105352
ATP2B1
12 89632685 intron variant G/A snv 0.14 4
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs111478946
ATP2B1
12 89665065 intron variant G/A snv 0.14 4
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs112862634
LINC00461 ; MEF2C-AS2
5 88674534 intron variant G/C snv 0.17 3
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs11867410
APOH
17 66231245 intron variant T/C snv 4.0E-02 3
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
rs12579720
LINC02398
12 20020830 intron variant C/A;G;T snv 2
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs1275982
KCNK3
2 26696221 intron variant C/T snv 0.48 3
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 3
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5