Disease: Mean blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs12579720
LINC02398
12 20020830 intron variant C/A;G;T snv 2
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs12790427
PCNX3
11 65617256 synonymous variant C/G;T snv 1.7E-05; 0.25 3
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs1502284
ARHGAP42
11 100713419 intron variant T/A;G snv 2
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs2125067
GDF10
10 47304942 intron variant G/A;C;T snv 3
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2990220
GBAP1
1 155220463 intron variant T/A;C;G snv 3
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4