Disease: Mean blood pressure
Source: INFERRED ×
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
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10826334 10 59620724 intron variant C/A;G snv 3
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs1105955 6 126826023 intron variant T/A snv 0.44 3
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
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
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs112862634
LINC00461 ; MEF2C-AS2
5 88674534 intron variant G/C snv 0.17 3
rs112913898 10 103199143 intergenic variant G/A snv 9.1E-02 3
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs1173727 5 32830415 intergenic variant T/C snv 0.66 4
rs1173766 5 32804422 intergenic variant T/C snv 0.57 4
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 8
rs1177765 5 32829823 intergenic variant T/C snv 0.50 3
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 4
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs1275982
KCNK3
2 26696221 intron variant C/T snv 0.48 3
rs1275984 2 26688641 upstream gene variant A/C;G snv 4