Disease: Diastolic blood pressure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5