Disease: C-reactive protein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17